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Submission Form to Bibliographic Databases

2017-09-20T09:37:00+02:00

JOURNAL SUBMISSION FORM

Title: Atlas of Genetics and Cytogenetics in Oncology and Haematology
URL: http://AtlasGeneticsOncology.org

I- Editor and Publisher

Editor-in-Chief: Jean-Loup Huret, Genetics, University Hospital of Poitiers; Database Director: Philippe Dessen, UMR 1170 INSERM, Gustave Roussy.

Second Editor handling manuscripts: Gajanan V Sherbet, Institute for Molecular Medicine at Huntington Beach California.

Contact Address: Jean-Loup Huret, MD, PhD, 10 rue des Treilles, Masseuil, F-86190 Quinçay, France / Gajanan Sherbet, School of Electrical Electronic and Computer Engineering University of Newcastle upon Tyne, UK

Email: jean-loup.huret@chu-poitiers.fr; jlhuret@univ-poitiers.fr; jean-loup.huret@atlasgeneticsoncology.org; / gajanan.sherbet@newcastle.ac.uk

Phone: +33 5 49 60 46 54

Publisher Address: INIST-CNRS, Catherine Morel, 2,Allée du Parc de Brabois, CS 10130, 54519 Vandoeuvre-lès-Nancy France.

Country of origin: France

e-ISSN: ISSN 1768-3262

Publishing Company: ARMGHM, a non-profit organisation, and by the Institute for Scientific and Technical Information of the French National Center for Scientific Research (INIST-CNRS) since 2008.

Funding: see "Activity reports" of the association in charge of the financial side: http://chromosomesincancer.org/en/activity.html

Sponsoring Organizations, Grants and past Grants: Scientific Societies; European funds; French Ministry of Higher Education and Research; Poitiers University Fundation; French National League against Cancer, etc… see http://atlasgeneticsoncology.org/BackpageAbout.html#GRANTS

II- Publishing Standards

Subject Area: Life Sciences

Publishing Format: electronic format.

Language of Journal: English

Open Access Journal: The Atlas is accessible, free, and may be reproduced under certain conditions (see http://atlasgeneticsoncology.org/BackpageAbout.html#COPYRIGHT and, in this paragraph, the hyperlink toward https://creativecommons.org/licenses/by-nc-nd/2.0/fr/deed.en_GB). Pages can be printed and/or recorded in ".html".

No fees for the authors; The Atlas is in open free access for readers, and there are no fees for the authors (the opposite of "predatory open access publishing").

1st Year of Publication: 1997

Issues Frequency: Continuous online: 12 issues per year

Periodicity: The journal publishes articles online one at a time rather than collecting articles for release as an "issue". We can nonetheless determine "issues" by chronology: months and years, see http://atlasgeneticsoncology.org/Recent.html and the archives, from 1997 (vol.1), to 2017 (vol.21): http://atlasgeneticsoncology.org/DatabaseArchives/DatabaseArchives.html

Regular and stable publication: The Atlas is a regular and uninterrupted publication since 1997.

Database Archives: http://atlasgeneticsoncology.org/DatabaseArchives/DatabaseArchives.html

Statistic of Authors by country: http://atlasgeneticsoncology.org/Status/Status_country.html

Bibliographic records: MetaData for bibliographic records of the Atlas are at the following URL: http://atlasgeneticsoncology.org/Collab/AtlasMetadata.txt with:TITLE/DATE AUTHORS/AFFILIATION/COUNTRY/CITATION /ABSTRACT/KEYWORDS / ATLAS_ID/CLASS(Section)/URL /PUBLICATION/PUBLISHER/ISSN/LANGUAGE

III- Editorial policies

Editorial policies can be found at the following address: http://atlasgeneticsoncology.org/BackpageAuthors.htmlwith more detailed pages:

Instructions to Authors: http://documents.irevues.inist.fr/bitstream/handle/2042/48486/Instructions-to-authors.pdf

Peer Review: http://documents.irevues.inist.fr/bitstream/handle/2042/56068/Policies-editorial-ethics.pdf

Ethical Publishing Practices: http://documents.irevues.inist.fr/bitstream/handle/2042/56068/Policies-editorial-ethics.pdf

Copyright/sponsorship: http://documents.irevues.inist.fr/bitstream/handle/2042/48487/Copyright-sponsorship.pdf

Editorial content: http://atlasgeneticsoncology.org/Status/Status.html

International focus: Concerning Section Editors and Board members: http://atlasgeneticsoncology.org/BackpageAbout.html#EDITORIAL ; Concerning Authors /papers by country: http://atlasgeneticsoncology.org/Status/Status_country.html ; Concerning internauts/readers: http://chromosomesincancer.org/en/atlas-users.html

IV- Quality of its contents and editorial processes

Aims and Scope of Journal: The Atlas of Genetics and Cytogenetics in Oncology and Haematology is a journal focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases.

Content: The Atlas contains 6 sections, with articles on: 1- Genes, 2- Leukemia entities, 3- Solid tumors, 4- Cancer-prone diseases, 5- 'Deep Insights' (articles dealing with topics in areas related to core subjects in the Atlas) 6- Case reports on hematological malignancies. Papers from sections 1 to 5 are review articles, all of them are commissioned papers. Section 6, case reports, are unsolicited papers.

Number of Reviewers Assigned per Manuscript: Commissioned papers (Review articles): 2 inside reviewers; Case Reports; 1 inside + 3 to 4 outside reviewers.

Percent of Commissioned vs. Unsolicited Manuscripts: 97% (Review articles i.e. all the papers except the Case Reports) vs. 3% (Case Reports)

Acceptance Rate of Unsolicited Manuscripts in last 12 months: accepted without revision: 8%; after revision: 68%; refused: 24%.

Average Time from Acceptance of Manuscript to Publication: 2-3 weeks

Article Types Published: Reviews: about 2650 papers; Research articles: 0 (NO research papers); Case Reports: about 90 papers).

Quality of its contents/Citations: Papers published in the Atlas are cited as such in: Annual Review of Biochemistry (Impact Factor 29,88), Science (29,75), Nature Reviews Cancer (29,54), Cancer Cell (25,29), Nature Cell Biology (19,53), Journal of the National Cancer Institute (14,07), American Journal of Human Genetics (12,30), Molecular Systems Biology (12,13), Genes and Development (12,08), Genome Research (11,34), Trends in Molecular Medicine (11,05), Blood (10,56), Proceedings of the National Academy of Sciences USA (9,43), Trends in Genetics (8,69), Leukemia (8,30), Cancer Res (7,54), Nucleic Acids Research (7,48), Oncogene (7,13), … and many others.
See also the statistics of Atlas users: http://chromosomesincancer.org/en/atlas-users.html
Acknowledgements: http://chromosomesincancer.org/en/acknoledgements-to-the-atlas.html
and "Nominated for award"http://chromosomesincancer.org/en/nominated-for-an-award.html

Templates_for_cards-papers

2017-09-14T14:29:56+02:00

TEMPLATES

TEMPLATE for GENES

Field	Syntax	Comment
BEGIN_HEADER
FILENAME	<Symbol>IDxxxch<location>.txt
CLASSE GENE	fixed
ID	A number (in the catalog)	Atlas ID
LOCUSID	number	Entrez ID
TRI_PAR_CHROMOSOME	chrom number (X Y, 1-22)
TRANSLOC
FUSION_GENE
CATEGORY	from a list of categories
END_HEADER

BEGIN_AUTHOR
CREATED DATE date AUTHORS authors	DATE YYYY-MM AUTHORS FirstName LastName, ..	separated by ","
CITATION	LastName Firstname Initial,	separated by ","
AUTHOR_AFFILIATION	(address, town, country, e-mail) ;
UPDATED DATE date AUTHORS authors	same syntax
CITATION		multiple of 3 lines in order of date
AUTHOR_AFFILIATION
END_AUTHOR

BEGIN_ABSTRACT
ABSTRACT		One line. Several lines with repeated Field
KEYWORDS		separation by ;
END_ABSTRACT

BEGIN_IDENTITY_GENE
NAME	<symbol> (description)
ALIAS	1 alias by line .	repeatable
HGNC	HGNC symbol
LOCATION	chromosomal band (as hg38 in UCSC)
LOCATION_BASE_PAIR	coordonates
LOCAL_ORDER
IMAGE	reference to a jpg, png .. Image	The images are saved in a sub directory Images
IMAGE_LEGEND
IMAGE_FISH
IMAGE_FISH_LEGEND
NOTE
END_IDENTITY_GENE

BEGIN_DNA_DESCRIPTION
NOTE
IMAGE
IMAGE_LEGEND
IMAGE_2
IMAGE_2_LEGEND
LINK_IMAGE
LINK_IMAGE_LEGEND
DESCRIPTION	txt
TRANSCRIPTION	txt
PSEUDOGENE	txt
END_DNA_DESCRIPTION

BEGIN_PROTEIN_DESCRIPTION
NOTE	txt
IMAGE
IMAGE_LEGEND
DESCRIPTION	txt
IMAGE_2
IMAGE_2_LEGEND
EXPRESSION	txt
IMAGE_3
IMAGE_3_LEGEND
LOCALISATION	txt
IMAGE_4
IMAGE_4_LEGEND
FUNCTION	txt
IMAGE_5
IMAGE_5_LEGEND
HOMOLOGY
IMAGE_6
IMAGE_6_LEGEND
IMAGE_7
IMAGE_7_LEGEND
END_PROTEIN_DESCRIPTION

BEGIN_MUTATIONS
NOTE	txt
IMAGE
IMAGE_LEGEND
IMAGE_2
IMAGE_2_LEGEND
IMAGE_3
IMAGE_3_LEGEND
IMAGE_VIGNETTE
IMAGE_VIGNETTE_LEGEND
GERMINAL	txt
SOMATIC	txt
EPIGENETICS	txt
END_MUTATIONS

BEGIN_IMPLICATED_IN
TOP_NOTE

BEGIN_ENTITY	repeatable bloc
ENTITY_NAME	<CC: TXT: Breast cancer ID: 5018>
NOTE	txt
DISEASE	txt
PROGNOSIS	txt
CYTOGENETICS	txt
HYBRID_GENE	txt
HYBRID_GENE_IMAGE
HYBRID_GENE_IMAGE_LEGEND
FUSION_PROTEIN	txt
FUSION_PROTEIN_IMAGE
FUSION_PROTEIN_IMAGE_LEGEND
ONCOGENESIS	txt
END_ENTITY

END_IMPLICATED_IN

BEGIN_BREAKPOINTS
IMAGE_PARTNERS
IMAGE_PARTNERS_LEGEND
IMAGE
IMAGE_LEGEND
NOTE	txt
END_BREAKPOINTS

BEGIN_TO_BE_NOTED
NOTE	txt
IMAGE
IMAGE_LEGEND
END_TO_BE_NOTED

BEGIN_EXTERNAL_LINKS
HUGO
GENECARD
GDBID
LOCUSLINK	Entrez Symbol	The only Field required
GENBANK		All the other Fields are fullfilled by a script and parallel informations
UNIGENE		defined in genes_gc.txt and genes_gn.txt
SWISSPROT
HGMD
OMIM
ORPHANET
REGISTRY
ASSOCIATIONS
PROBES
DATABASES
NOTE
END_EXTERNAL_LINKS

BEGIN_FULL_BIBLIOGRAPHY

BEGIN_REF	repeatable bloc	Actually references are ordered by fisrt author
TITLE		References are regenerated from PubMed by PMID value
AUTHORS
REFERENCE
PMID
END_REF

END_FULL_BIBLIOGRAPHY
///

II- TEMPLATE for LEUKEMIAS

Field	Syntax	Comment	Example
BEGIN_HEADER
FILENAME <Transloc>IDxxx.txt
CLASSE CHROM_CLIN	fixed
ID
STATUS
TRI_PAR_CHROMOSOME
TRI_CHROM			Examples: 01;19 for t(1;19); 16;00 for inv(16); 99;00 for "NA" (no chrom. Assigned)
TRANSLOC			Example: t(11;19)(q13;p13) FSTL3/CCND1
FUSION_GENE			Example: FSTL3/CCND1
CLASS_DISEASE	one or several values; one value per line	MPD, and/or MDS, t-AML, AML, B-ALL, T-ALL, NHL
ICD-O3_TOPO			C420,C421,C424
ICD-O3_MORPH
END_HEADER

BEGIN_AUTHOR
CREATED DATE date AUTHORS authors
CITATION
AUTHOR_AFFILIATION
UPDATED DATE date AUTHORS authors
CITATION
AUTHOR_AFFILIATION
END_AUTHOR

BEGIN_ABSTRACT
ABSTRACT
KEYWORDS
END_ABSTRACT

BEGIN_IDENTITY_CHROM_CLIN
NAME
ALIAS
NOTE
IMAGE
IMAGE_LEGEND
END_IDENTITY_CHROM_CLIN

BEGIN_CLINICS_AND_PATHOLOGY
NOTED

BEGIN_DISEASE
DISEASE
NOTE
PHENOTYPE_STEM_CELL_ORIGIN
EMBRYONIC_ORIGIN
ETIOLOGY
EPIDEMIOLOGY
CLINICS
CLINICS_IMAGE
CLINICS_IMAGE_LEGEND
CYTOLOGY_IMAGE
CYTOLOGY_IMAGE_LEGEND
CYTOLOGY
PATHOLOGY
PATHOLOGY_IMAGE
PATHOLOGY_IMAGE_LEGEND
PATHOLOGY_IMAGE_2
PATHOLOGY_IMAGE_2_LEGEND
PATHOLOGY_IMAGE_3
PATHOLOGY_IMAGE_3_LEGEND
PATHOLOGY_IMAGE_4
PATHOLOGY_IMAGE_4_LEGEND
PATHOLOGY_IMAGE_5
PATHOLOGY_IMAGE_5_LEGEND
PATHOLOGY_IMAGE_6
PATHOLOGY_IMAGE_6_LEGEND
PATHOLOGY_IMAGE_7
PATHOLOGY_IMAGE_7_LEGEND
PATHOLOGY_IMAGE_8
PATHOLOGY_IMAGE_8_LEGEND
PATHOLOGY_IMAGE_9
PATHOLOGY_IMAGE_9_LEGEND
PATHOLOGY_IMAGE_10
PATHOLOGY_IMAGE_10_LEGEND
PATHOLOGY_IMAGE_11
PATHOLOGY_IMAGE_11_LEGEND
PATHOLOGY_IMAGE_12
PATHOLOGY_IMAGE_12_LEGEND
OTHER_FEATURES
OTHER_FEATURES_IMAGE
OTHER_FEATURES_IMAGE_LEGEND
CYTOGENETICS
GENES
TREATMENT
EVOLUTION
PROGNOSIS
END_DISEASE

END_CLINICS_AND_PATHOLOGY

BEGIN_GENETICS
NOTE
GENETICS_IMAGE
GENETICS_IMAGE_LEGEND
GENETICS_IMAGE_2
GENETICS_IMAGE_2_LEGEND
GENETICS_IMAGE_3
GENETICS_IMAGE_3_LEGEND
END_GENETICS

BEGIN_CYTOGENET
NOTE
CYTOGENETICS_MORPHOLOGICAL_IMAGE
CYTOGENETICS_MORPHOLOGICAL_IMAGE_LEGEND
CYTOGENETICS_MORPHOLOGICAL
CYTOGENETICS_MOLECULAR
CYTOGENETICS_MOLECULAR_IMAGE
CYTOGENETICS_MOLECULAR_IMAGE_LEGEND
PROBES
ADDITIONAL_ANOMALIES
VARIANTS
END_CYTOGENET

BEGIN_GENES_AND_PROTEINS
NOTE
COMPLEMENTATION_GROUPS

BEGIN_GENE_SHORT
GENE_NAME
ID
LOCATION
NOTE
DNA_RNA_DESCRIPTION
IMAGE
IMAGE_LEGEND
PROTEIN_DESCRIPTION
GERMINAL_MUTATIONS
SOMATIC_MUTATIONS
END_GENE_SHORT

END_GENES_AND_PROTEINS

BEGIN_RESULT_OF_THE_CHROMOSOMAL_ANOMALY
BEGIN_HYBRID_GENE
NOTE
HYBRID_GENE_IMAGE
HYBRID_GENE_IMAGE_LEGEND
DESCRIPTION
TRANSCRIPT
DETECTION_PROTOCOLE
END_HYBRID_GENE

BEGIN_FUSION_PROTEIN
NOTE
FUSION_PROTEIN_IMAGE
FUSION_PROTEIN_IMAGE_LEGEND
DESCRIPTION
EXPRESSION_LOCALISATION
ONCOGENESIS
END_FUSION_PROTEIN

END_RESULT_OF_THE_CHROMOSOMAL_ANOMALY

BEGIN_TO_BE_NOTED
NOTE
IMAGE
IMAGE_LEGEND
CASE_REPORT
END_TO_BE_NOTED

BEGIN_EXTERNAL_LINKS
PROBES
DATABASES
NOTE
END_EXTERNAL_LINKS

BEGIN_FULL_BIBLIOGRAPHY

BEGIN_REF
TITLE
AUTHORS
REFERENCE
PMID
END_REF

END_FULL_BIBLIOGRAPHY
///

III- TEMPLATE for SOLID TUMORS

Field	Syntax
BEGIN_HEADER
FILENAME
CLASSE TUMOUR	fixed
ID
TRI_PAR_CHROMOSOME
TRI_CHROM
TRANSLOC
FUSION_GENE
ICD-O3_TOPO
ICD-O3_MORPH
END_HEADER

BEGIN_AUTHOR
CREATED DATE date AUTHORS authors
CITATION
AUTHOR_AFFILIATION
UPDATED DATE date AUTHORS authors
CITATION
AUTHOR_AFFILIATION
END_AUTHOR

BEGIN_ABSTRACT
ABSTRACT
KEYWORDS
END_ABSTRACT

BEGIN_IDENTITY_TUMOUR
NAME
ALIAS
PHYLUM_COMPLETE
PHYLUM_TISSUE_ORGAN
PHYLUM_DISEASE
NOTE
IMAGE
IMAGE_LEGEND
END_IDENTITY_TUMOUR

BEGIN_CLASSIFICATION
NOTE
IMAGE
IMAGE_LEGEND
CLASSIFICATION
END_CLASSIFICATION

BEGIN_CLINICS_AND_PATHOLOGY
NOTE

BEGIN_DISEASE
DISEASE
NOTE
PHENOTYPE_STEM_CELL_ORIGIN
EMBRYONIC_ORIGIN
ETIOLOGY
EPIDEMIOLOGY
CLINICS
CLINICS_IMAGE
CLINICS_IMAGE_LEGEND
CYTOLOGY_IMAGE
CYTOLOGY_IMAGE_LEGEND
CYTOLOGY
PATHOLOGY
PATHOLOGY_IMAGE
PATHOLOGY_IMAGE_LEGEND
PATHOLOGY_IMAGE_2
PATHOLOGY_IMAGE_2_LEGEND
PATHOLOGY_IMAGE_3
PATHOLOGY_IMAGE_3_LEGEND
OTHER_FEATURES
OTHER_FEATURES_IMAGE
OTHER_FEATURES_IMAGE_LEGEND
CYTOGENETICS
GENES
TREATMENT
EVOLUTION
PROGNOSIS
END_DISEASE

END_CLINICS_AND_PATHOLOGY

BEGIN_GENETICS
NOTE
GENETICS_IMAGE
GENETICS_IMAGE_LEGEND
GENETICS_IMAGE_2
GENETICS_IMAGE_2_LEGEND
GENETICS_IMAGE_3
GENETICS_IMAGE_3_LEGEND
END_GENETICS

BEGIN_CYTOGENET
NOTE
CYTOGENETICS_MORPHOLOGICAL_IMAGE
CYTOGENETICS_MORPHOLOGICAL_IMAGE_LEGEND
CYTOGENETICS_MORPHOLOGICAL
CYTOGENETICS_MOLECULAR
CYTOGENETICS_MOLECULAR_IMAGE
CYTOGENETICS_MOLECULAR_IMAGE_LEGEND
PROBES
ADDITIONAL_ANOMALIES
VARIANTS
END_CYTOGENET

BEGIN_GENES_AND_PROTEINS
NOTE
COMPLEMENTATION_GROUPS

BEGIN_GENE_SHORT
GENE_NAME
ID
LOCATION
NOTE
DNA_RNA_DESCRIPTION
IMAGE
IMAGE_LEGEND
PROTEIN_DESCRIPTION
GERMINAL_MUTATIONS
SOMATIC_MUTATIONS
END_GENE_SHORT

END_GENES_AND_PROTEINS

BEGIN_RESULT_OF_THE_CHROMOSOMAL_ANOMALY
BEGIN_HYBRID_GENE
NOTE
HYBRID_GENE_IMAGE
HYBRID_GENE_IMAGE_LEGEND
DESCRIPTION
TRANSCRIPT
DETECTION_PROTOCOLE
END_HYBRID_GENE

BEGIN_FUSION_PROTEIN
NOTE
FUSION_PROTEIN_IMAGE
FUSION_PROTEIN_IMAGE_LEGEND
DESCRIPTION
EXPRESSION_LOCALISATION
ONCOGENESIS
END_FUSION_PROTEIN

END_RESULT_OF_THE_CHROMOSOMAL_ANOMALY

BEGIN_TO_BE_NOTED
NOTE
IMAGE
IMAGE_LEGEND
END_TO_BE_NOTED

BEGIN_EXTERNAL_LINKS
PROBES
DATABASES
NOTE
END_EXTERNAL_LINKS

BEGIN_FULL_BIBLIOGRAPHY

BEGIN_REF
TITLE
AUTHORS
REFERENCE
PMID
END_REF

END_FULL_BIBLIOGRAPHY
///

IV- TEMPLATE for CANCER-PRONE DISEASES

Field	Syntax	Comment	Example
BEGIN_HEADER
FILENAME
CLASSE K_PRONE	fixed
ID		Atlas_ID
TRI_PAR_CHROMOSOME
LOCATION
GENES_INVOLVED
OMIM
END_HEADER

BEGIN_AUTHOR
CREATED DATE date AUTHORS authors
CITATION
AUTHOR_AFFILIATION
UPDATED DATE date AUTHORS authors
CITATION
AUTHOR_AFFILIATION
END_AUTHOR

BEGIN_ABSTRACT
ABSTRACT
KEYWORDS
END_ABSTRACT

BEGIN_IDENTITY_K_PRONE
NAME
ALIAS
NOTE
INHERITANCE
IMAGE
IMAGE_LEGEND
END_IDENTITY_K_PRONE

BEGIN_CLINICS
NOTE
PHENOTYPE_AND_CLINICS
IMAGE_1
IMAGE_1_LEGEND
IMAGE_2
IMAGE_2_LEGEND
DIFFERENTIAL_DIAGNOSIS
IMAGE_3
IMAGE_3_LEGEND
NEOPLASTIC_RISK
TREATMENT
EVOLUTION
PROGNOSIS
END_CLINICS

BEGIN_CYTOGENETICS
NOTE
INBORN_CONDITION
IMAGE
IMAGE_LEGEND
ACQUIRED_CONDITION
ACQUIRED_CONDITION_IMAGE
ACQUIRED_CONDITION_IMAGE_LEGEND
END_CYTOGENETICS

BEGIN_OTHER_FINDINGS
NOTE
END_OTHER_FINDINGS

BEGIN_GENES_AND_PROTEINS
NOTE
COMPLEMENTATION_GROUPS

BEGIN_GENE
GENE_NAME			<CC: TXT: BRCA1 ID: 11111>
ID			11111
LOCATION			25q23.4
NOTE
END_GENE

BEGIN_DNA_DESCRIPTION
NOTE
IMAGE
IMAGE_LEGEND
DNA_DESCRIPTION
TRANSCRIPTION
PSEUDOGENE
END_DNA_DESCRIPTION

BEGIN_PROTEIN_DESCRIPTION
NOTE
IMAGE
IMAGE_LEGEND
DESCRIPTION
EXPRESSION
LOCALISATION
FUNCTION
HOMOLOGY
END_PROTEIN_DESCRIPTION

BEGIN_MUTATIONS
NOTE
IMAGE
IMAGE_LEGEND
GERMINAL
SOMATIC
EPIGENETICS
END_MUTATIONS

END_GENES_AND_PROTEINS

BEGIN_TO_BE_NOTED
NOTE
IMAGE
IMAGE_LEGEND
CASE_REPORT
END_TO_BE_NOTED

BEGIN_EXTERNAL_LINKS
HGMD
OMIM
ORPHANET
REGISTRY
ASSOCIATIONS
DATABASES
NOTE
END_EXTERNAL_LINKS

BEGIN_FULL_BIBLIOGRAPHY

BEGIN_REF
TITLE
AUTHORS
REFERENCE
PMID
END_REF

END_FULL_BIBLIOGRAPHY
///

Atlas Submission to Bibliographic Databases

2017-08-25T09:29:44+02:00

JOURNAL SUBMISSION FORM

Title: Atlas of Genetics and Cytogenetics in Oncology and Haematology

Journal: http://irevues.inist.fr/atlasgeneticsoncology

Note: the Journal papers are also available as a Database: http://AtlasGeneticsOncology.org

I- Editor and Publisher

Editors-in-Chief:
Jesús María Hernández Rivas (Molecular Cytogenetics Lab, Dept. of Hematology, University Hospital of Salamanca, Spain
Paola Dal Cin Professor, Pathology, Harvard Medical School, Cytogeneticist, Cytogenetics Laboratory, Brigham And Women's Hospital, Boston, MA 02215
Jean-Loup Huret, Honorary Associate Professor of Medical Genetics of the French Universities.

Contact Address: Jean-Loup Huret, MD, PhD, 10 rue des Treilles, Masseuil, F-86190 Quinçay, France.

Email: jean-loup.huret@chu-poitiers.fr; jlhuret@univ-poitiers.fr; jean-loup.huret@atlasgeneticsoncology.org; / anaerv@hotmail.com; teresa.gonzalez@mundo-r.com

Phone: +33 5 49 60 46 54

Publisher Address: INIST-CNRS, Catherine Morel, 2,Allée du Parc de Brabois, CS 10130, 54519 Vandoeuvre-lès-Nancy France.

Country of origin: France

e-ISSN: ISSN 1768-3262

Publishing Company: ARMGHM, a non-profit organisation, and by the Institute for Scientific and Technical Information of the French National Center for Scientific Research (INIST-CNRS) since 2008.

Funding: see "Activity reports" of the association in charge of the financial side: http://chromosomesincancer.org/en/activity.html

Sponsoring Organizations, Grants and past Grants: Scientific Societies; European funds; French Ministry of Higher Education and Research; French National League against Cancer, etc… see http://atlasgeneticsoncology.org/BackpageAbout.html#GRANTS

II- Publishing Standards

Subject Area: Life Sciences

Publishing Format: electronic format.

Language of Journal: English

No fees for the authors; The Atlas is in open free access for readers, and there are no fees for the authors (the opposite of "predatory open access publishing").

1st Year of Publication: 1997

Issues Frequency: Continuous online: 12 issues per year

Periodicity: The database publishes articles online one at a time and articles are collected for release as "issues" and "volumes" for the Journal, see http://irevues.inist.fr/atlasgeneticsoncology (see also the archives of the database at http://atlasgeneticsoncology.org/DatabaseArchives/DatabaseArchives.html).

Regular and stable publication: The Atlas is a regular and uninterrupted publication since 1997.

Most Recent Issue (Vol, Iss, Yr): As today, Volume 22, 2018, December, issue 12, 9 articles.

Journal Archives: http://irevues.inist.fr/atlasgeneticsoncology (database archives: http://atlasgeneticsoncology.org/DatabaseArchives/DatabaseArchives.html).

Statistic of Authors by country: http://atlasgeneticsoncology.org/Status/Status_country.html

Bibliographic records: MetaData for bibliographic records of the Atlas Journal are handled by CNRS-INIST are at the following URL: http://irevues.inist.fr/atlasgeneticsoncology and may be uploaded upon request (see also MetaData in the database at; http://atlasgeneticsoncology.org/Collab/AtlasMetadata.txt).

III- Editorial policies

Editorial policies can be found at the following addresses:

Instructions to Authors: http://documents.irevues.inist.fr/bitstream/handle/2042/48486/Instructions-to-authors.pdf

Peer Review: http://documents.irevues.inist.fr/bitstream/handle/2042/56068/Policies-editorial-ethics.pdf

Ethical Publishing Practices: http://documents.irevues.inist.fr/bitstream/handle/2042/56068/Policies-editorial-ethics.pdf

Copyright/sponsorship: http://documents.irevues.inist.fr/bitstream/handle/2042/48487/Copyright-sponsorship.pdf

Editorial content: http://atlasgeneticsoncology.org/Status/Status.html

IV- Quality of its contents and editorial processes

Number of Reviewers Assigned per Manuscript: Commissioned papers (Review articles): 2 inside reviewers; Case Reports; 1 inside + 3 to 4 outside reviewers.

Percent of Commissioned vs. Unsolicited Manuscripts: 97% (Review articles i.e. all the papers except the Case Reports) vs. 3% (Case Reports)

Acceptance Rate of Unsolicited Manuscripts in last 12 months: accepted without revision: 8%; after revision: 68%; refused: 24%.

Average Time from Acceptance of Manuscript to Publication: 2-3 weeks

Article Types Published: Reviews: about 2650 papers; Research articles: 0 (NO research papers); Case Reports: about 90 papers).

MainScriptsofAtlas

2017-08-25T07:54:29+02:00

# ##################################################
# A. General pipeline for updating the Atlas       #
# ##################################################
# 2017-07-29 Dessen Philippe (dessen@igr.fr)
#
# all scripts are running in $CYT_DIR/Scripts directory
#
#!/usr/bin/bash
# ===============================================================
# AUTHOR : P. DESSEN
# DATE   : Mon Aug 2 18:27:27 MET DST 1999
# FILE   : maj_full.sh
# GOAL   : Automatic updating of html files from txt files
# RUN : ./maj_full.sh 2>/dev/null > indexation.log &
# ===============================================================
cd $CYT_DIR/Scripts
date1=`date`
echo "start " $date1
# I. Generation of Genes links from Anomalies, Tumors, Kprones
# =============================================================
# Identification of all links (CC: TXT: ID: > in all txt files

./ident_hyper.pl

# Generation of several files
# hyper_Genes0.txt
# hyper_Anomalies.txt
# hyper_Tumors.txt
# hyper_Kprones.txt
# followed by concatenation in ./Scripts/Data/hyper_All.txt
# creation of Data if does exist

./otheranom_gene2.pl

# otheranom_gene2.pl in Scripts
# creation of an html bloc in Genes html_files
# with relation with Anomalies files
# Generation of id.html files in the directory
# ../Genes/AnomLinks/1.html
# 2 distinct extracts
# 1. genes associated with a FUSION_GENE in Anom files
# 2. genes associated with Anom in hyperlinks <CC: TXT: ID:>
# use the file ./Data/hyper_All.txt
# and the file ./genes_gc.txt (indexation of filename with NAME)

./othertumor_gene2.pl

# othertumor_gene.pl dans Scripts
# creation of an html bloc in Genes html_files
# with relation with Tumors files
# Generation of id.html files in the directory
# ../Genes/TumorsLinks/1.html
# 2 distinct extracts
# 1. genes associated with FUSION_GENE in the Tumors files
# 2. genes associated with Tumors in hyperlinks <CC: TXT: ID:>

./otherkprone_gene2.pl

# otherkprone_gene2.pl in Scripts
# creation of an html bloc in Genes html_files
# Generation of id.html files in the directory
# ../Genes/KpronesLinks/10001.html
# 2 distinct extractions
# 1. genes associated with SYMBOL dans les fiches Kprones
# 2. genes associated with Kprones in hyperlinks <CC: TXT: ID:>

./othergene_anom.pl
# othergene_anom.pl id_chrom_clin in Scripts
# creation of a html bloc html for Anomalies
# in the directory
# ../Anomalies/GeneLinks/1001.html

./othertransloc_anom.pl

# othertransloc_anom.pl in Scripts
# creation of a transloc html bloc for Anomalies
# Validation in first the creation of the fil
#   ./Data/hyper_translocAll.txt
# with the script extract_transloc_name.pl
#
# Generation of links files of transloc files with Anomalies
# File created by extract_transloc_name.pl from
# ./Data/hyper_translocAll.txt

./othergene_tumor.pl

# othergene_tumor.pl dans Scripts
# uses the file ./Data/hyper_All.txt
# creation of an html bloc for    Tumors in
#   ../Tumors/GeneLinks/5001.html
# Generation of links of Genes files with Tumors
# File created by extract_gene_name.pl from
# ./Data/hyper_All.txt
#
require "./miscfct.pl"; # fonctions diverses
require "gereDbid.pl"; # -- pour l'id des genes

./cytatlas
$ ls -ld */*Links
drwxrwxr-x+ 1 phd None 0 1 juil. 09:28 Anomalies/GeneLinks
drwxrwxr-x+ 1 phd None 0 1 juil. 09:24 Genes/AnomLinks
drwxrwxr-x+ 1 phd None 0 1 juil. 09:27 Genes/KproneLinks
drwxrwxr-x+ 1 phd None 0 1 juil. 09:27 Genes/TumorLinks
drwxrwxr-x+ 1 phd None 0 1 juil. 09:28 Tumors/GeneLinks

#
# II. Generation of Genes txt and html files
# ==========================================
rm ../Genes/GC_*.txt
rm -f ../../chromcancer/Genes/GC_*.html

# for the 2 sets of non annotated genes
./gen_genes_gn.sh
./gen_genes_gc.sh
# for the set of experted genes (Genes0)

./gen_gene2.sh

# creation of links from GC_annot_genes to AtlasFilename
# This permits to address url either bt AtlasFilename or by
# symolic url "GC_<symbol>.html"

./gen_genes_link.sh
#
# III. indexation
# ===============
./indexation.sh
#
# IV. Generation of all html files
# ================================
# preliminary
# generation of preliminary files LK_xxx.html , TU_xxx.html ..
# for forsale files

./maj_prelim.sh
#
# generation of html cards files
./gen_anom.sh
./gen_kprone.sh
./gen_tumor.sh
./gen_report.sh
./gen_educ.sh
./gen_deep.sh
#./gen_study.sh

# chromosome pages indexation
./index_bychrom3.pl

# reindexation (second round : not mandatory ?)
./indexation.sh
# regeneration of html cards (after reindexation)
./gen_gene2.sh
./gen_anom.sh
./gen_kprone.sh
./gen_tumor.sh
./gen.educ.sh
./gen_deep.sh
./gen_report.sh

# Management of images
cp_anom_img.sh
cp_deep_img.sh
cp_educ_img.sh
cp_genes_img.sh
cp_kpr_img.sh
cp_report_img.sh
cp_tum_img.sh
date2=`date`
echo "end " $date2
echo "maj_full.sh " $date1   $date2
echo "==================================="
#
mail -s "Atlas_IGR__maj_full " dessen@igr.fr < nohup.out
mail -s "Atlas_IGR__maj_full " dessen@igr.fr < indexation.log

# ##################################
# B. Indexation procedure          #
# ##################################

# Use indexation.sh after any modifications on cards to maintain
# updated indexes and links

# indexation.sh

#!/bin/bash
# ==============================================================
# AUTHOR : P.DESSEN
# DATE   : 11.12.99
# FILE   :./indexation.sh
# GOAL   : automatic generation of indexes and catalogs
# ex: ./indexation.sh 2 >/dev/null > indexation_20160306.log &
# to be run in $CYT_DIR/Scripts
# ==============================================================
# ------------------------------------------------
# ATLAS environnement variables
# ------------------------------------------------
# CYT_DIR needs to be defined (in $HOME/cytatlas.sh)
# CYT_DIR='..'
source $HOME/cytatlas.sh
GENE_DIR=$CYT_DIR/Genes
ANOM_DIR=$CYT_DIR/Anomalies
TUMOR_DIR=$CYT_DIR/Tumors
KPRON_DIR=$CYT_DIR/Kprones
REPORT_DIR=$CYT_DIR/Reports
STUDY_DIR=$CYT_DIR/StudyGroup
DEEP_DIR=$CYT_DIR/Deep
EDUC_DIR=$CYT_DIR/Educ
WGENE_DIR=$CYTW_DIR/Genes
WANOM_DIR=$CYTW_DIR/Anomalies
WTUMOR_DIR=$CYTW_DIR/Tumors
WKPRON_DIR=$CYTW_DIR/Kprones
WREPORT_DIR=$CYTW_DIR/Reports
WDEEP_DIR=$CYTW_DIR/Deep
WEDUC_DIR=$CYTW_DIR/Educ
WCOLLAB_DIR=$CYTW_DIR/Collab
SCRIPT_DIR=$CYT_DIR/Scripts
export GENE_DIR ANOM_DIR TUMOR_DIR KPRON_DIR SCRIPT_DIR
export REPORT_DIR STUDY_DIR DEEP_DIR EDUC_DIR
export WGENE_DIR WANOM_DIR WTUMOR_DIR WKPRON_DIR
export WREPORT_DIR WDEEP_DIR WEDUC_DIR WCOLLAB_DIR
# ----------------------------------------------
echo "--------------------------------------------------------"
echo " Atlas indexation
echo "`date`
echo "--------------------------------------------------------"
DATEIN=`date`
# pretraitment
# Regeneration of GC.txt files_
echo "Generation of GC_xxx.txt files "
echo "the genes_gc.txt and genes_gn.txt files need to be updated\n"
perl $CYT_DIR/Scripts/gener_gc.pl genes_gc.txt 2>/dev/null
perl $CYT_DIR/Scripts/gener_gc.pl genes_gn.txt 2>/dev/null
ls -l genes_gc.txt
ls -l genes_gn.txt
# ----------------------------------------------------------
# Build of the database of all objects of Atlas
#   ObjDB.txt contains the list
# ----------------------------------------------------------
echo "Build of the database ObjDB.txt"
echo "`date`";
perl $CYT_DIR/Scripts/x_id.pl # build if ObjDB.txt
ls -l ObjDB.txt
# ----------------------------------------------------------
# Build of the Genes : file ObjDB0.txt
perl $CYT_DIR/Scripts/majgene.pl 2>/dev/null       #
ls -l ObjDB0.txt
# ----------------------------------------------------------
# catalog maintains several features of each card
echo "Creation of a catalog"
perl $CYT_DIR/Scripts/catalog.pl   2>/dev/null      #
ls -l catalog
# ----------------------------------------------------------
# reconstruction des index divers
echo "Build of ObjDB1.txt and ObjDB2.txt"
perl $CYT_DIR/Scripts/majfich.pl    2>/dev/null     #
ls -l ObjDB1.txt
ls -l ObjDB2.txt
echo "Build of ObjDB1.html"
perl $CYT_DIR/Scripts/majfich2.pl   2>/dev/null     #
echo "Build of ObjDB3.txt and ObjDB4.txt"
perl $CYT_DIR/Scripts/majfich3.pl    2>/dev/null     #
ls -l ObjDB3.txt
ls -l ObjDB4.txt
echo "Build of ObjDB5.txt (correlation anom tumor genes) and ObjDB7.txt"
perl $CYT_DIR/Scripts/majfich5.pl 2>/dev/null
ls -l ObjDB5.txt
# ----------------------------------------------------------
# Generation of tabulated files for catalog and forsale
# catalog_out.txt and forsale_out.txt
perl $CYT_DIR/Scripts/forsale_out.pl forsale 2>/dev/null   # perl $CYT_DIR/Scripts/forsale_out.pl catalog 2>/dev/null   #
ls -l forsale_out.txt
ls -l catalog_out.txt
# ----------------------------------------------------------
# modification of catalog_out.txt depending of the reserved file
perl $CYT_DIR/Scripts/reserved.pl
# ----------------------------------------------------------
# concatenation of catalogs (catalog + forsale)
cat $CYT_DIR/Scripts/catalog_out.txt > catalog_full.txt
cat $CYT_DIR/Scripts/forsale_out.txt >> catalog_full.txt
ls -l catalog_full.txt
# Generation of a expertized Gene file
grep GENE ../../chromcancer/Collab/catalog_out.txt | awk -F\t '{print $3,"\t",$5} ' |grep -v GC_ > gce.txt
# ----------------------------------------------------------
#
echo "============= End of rebuild ================"
# ----------------------------------------------------------
# --- Indexations -----
# creation of several indexes for Genes
# index of genes by symbol
# index of objects by chromosome.
# ----------------------------------------------------------
echo " "
echo " --- Indexation des genes ---"
cd $GENE_DIR
$CYT_DIR/Scripts/index_gene2.pl 2>/dev/null   > $WGENE_DIR/Geneliste.html
ls -l $WGENE_DIR/Geneliste.html
cd $CYT_DIR/Scripts
$CYT_DIR/Scripts/index_genes_red.pl
echo " "
echo " --- Indexation of Anomalies ---"
$CYT_DIR/Scripts/index_anom2.pl 2>/dev/null    > $WANOM_DIR/Anomliste.html
$CYT_DIR/Scripts/index_lymphoma.pl 2>/dev/null > $WANOM_DIR/Lymphomaliste.html
$CYT_DIR/Scripts/index_myeloid.pl 2>/dev/null > $WANOM_DIR/Myeloidliste.html
ls -l $WANOM_DIR/Anomliste.html
ls -l $WANOM_DIR/Lymphomaliste.html
ls -l $WANOM_DIR/Myeloidliste.html
echo " "
echo " --- Indexation of Tumors ---"
cd $TUMOR_DIR
$CYT_DIR/Scripts/index_tumor2.pl 2>/dev/null > $WTUMOR_DIR/Tumorliste.html
ls -l $WTUMOR_DIR/Tumorliste.html
cd $CYT_DIR/Scripts
$CYT_DIR/Scripts/solid_section.pl 2>/dev/null
echo " "
echo " --- Indexation of Kprones ---"
cd $KPRON_DIR
$CYT_DIR/Scripts/index_kprone.pl 2>/dev/null   > $WKPRON_DIR/Kproneliste.html
ls -l $WKPRON_DIR/Kproneliste.html
echo " "
echo " --- Indexation of Reports ---"
cd $REPORT_DIR
$CYT_DIR/Scripts/index_report.pl 2>/dev/null   > $WREPORT_DIR/Reportliste.html
ls -l $WREPORT_DIR/Reportliste.html
echo " --- Indexation of Deep ---"
cd $DEEP_DIR
$CYT_DIR/Scripts/index_deep.pl 2>/dev/null   > $WDEEP_DIR/deeplist.html
ls -l $WDEEP_DIR/deeplist.html
cd $CYT_DIR/Scripts
chmod a+r $CYTW_DIR/Genes/Geneliste.html
chmod a+r $CYTW_DIR/Anomalies/Anomliste.html
chmod a+r $CYTW_DIR/Tumors/Tumorliste.html
chmod a+r $CYTW_DIR/Kprones/Kproneliste.html
chmod a+r $CYTW_DIR/Reports/Reportliste.html
chmod a+r $CYTW_DIR/Deep/deeplist.html
# ----------------------------------------------------------
#
## echo " "
## echo "--- Indexation of GeneLink ---"
####     Normally done in maj_full.sh #####
#### $CYT_DIR/Scripts/ident_hyper.pl
#### $CYT_DIR/Scripts/othergene_anom.pl
#### $CYT_DIR/Scripts/othergene_tumor.pl
#### $CYT_DIR/Scripts/othergene_kprone.pl
#### $CYT_DIR/Scripts/otheranom_gene2.pl
#### $CYT_DIR/Scripts/othertransloc_anom.pl
#### $CYT_DIR/Scripts/othertumor_gene2.pl
#### $CYT_DIR/Scripts/otherkprone_gene2.pl
# ----------------------------------------------------------
#
echo " "
echo " --- Mitelman Files ---"
cd $CYT_DIR/Scripts
$CYT_DIR/Scripts/report2mitelman.pl 2> /dev/null
$CYT_DIR/Scripts/report2mitelman2.pl2> /dev/null
$CYT_DIR/Scripts/a0_mitel2jlh.pl > ../../chromcancer/Collab/mitelman_anom.txt
echo ""
# ----------------------------------------------------------
#
#echo " ----- Indexation of Genes GC --- "
#cd $CYT_DIR/Scripts
#perl $CYT_DIR/Scripts/index_genes_gc.sh
# ----------------------------------------------------------
#
echo " "
echo " --- Indexation by chrom ---"
cd $CYT_DIR/Scripts
perl $CYT_DIR/Scripts/index_bychrom3.pl 2> /dev/null
perl $CYT_DIR/Scripts/index_genes_chromg.pl 2>/dev/null
echo " "
echo " --- Creation of th file cytoentities.html ---"
perl $CYT_DIR/Scripts/cytoentities.pl 2> /dev/null
perl $CYT_DIR/Scripts/cytoentities2.pl 2> /dev/null
# ----------------------------------------------------------
### echo " --- Indexation of the file hugo2url.dat ---"
### perl $CYT_DIR/Scripts/hugo2url.pl
# ----------------------------------------------------------
echo " "
echo " --- Creation of file GeneExtlnk.txt ---"
perl $CYT_DIR/Scripts/extlnk2.pl Genes 2>/dev/null
echo " "
echo " --- Creation of file GeneExtlnk.html ---"
perl $CYT_DIR/Scripts/extlnk3.pl Genes 2>/dev/null
echo " "
echo " --- Creation of file GeneLink.txt ---"
perl $CYT_DIR/Scripts/extlnk4.pl Genes
# ----------------------------------------------------------
## indexation des authors
cd $CYT_DIR/Scripts
perl indxauth.pl 2>/dev/null
ls -l IndxAuth.txt
perl indxauth2.pl 2>/dev/null
ls -l indxauth2.pl
ls -l IndxAuth.html
ls -l IndxAuth2.txt
echo "Be careful : the key_date_pays.txt file may be updated...."
ls -l key_date_pays.txt
echo "Indexation IndxAuth3.txt "
perl indxauth3.pl 2>/dev/null
ls -l IndxAuth3.txt
echo "Indexation IndxAuth4.txt "
perl traitauth.pl 2>/dev/null > ./IndxAuth4.txt
ls -l IndxAuth4.txt
echo "Indexation IndxAuth5.txt "
perl indxauth5.pl 2>/dev/null
ls -l IndxAuth5.txt
echo "Indexation IndxAuth6.txt "
perl indxauth6.pl 2>/dev/null
ls -l IndxAuth6.txt
echo "Indexation IndxAuth1.txt "
perl indxauth1.pl 2>/dev/null
ls -l IndxAuth1.txt
## copies of authors indexes in Collab (Archive)
echo "mv to ../../chromcancer/Collab "
mv IndxAuth.txt   $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth.txt
mv IndxAuth.html $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth.html
mv IndxAuth2.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth2.txt
mv IndxAuth2.html $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth.html
mv IndxAuth3.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth3.txt
mv IndxAuth4.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth4.txt
mv IndxAuth5.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth5.txt
mv IndxAuth6.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth6.txt
mv IndxAuth1.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth1.txt
mv IndxAuth1.html $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxAuth1.html
cp -p key_date_pays.txt   $CYTW_DIR/Collab
# ----------------------------------------------------------
# Generation of Nosology
echo "Reconsruction des Nosology"
perl $CYT_DIR/Scripts/solid_nosology2.pl 2>/dev/null
ls -l $CYTW_DIR/Tumors/Solid_Nosol*.html
# ----------------------------------------------------------
## indexation des images
echo "Indexation of images"
perl $CYT_DIR/Scripts/indximg.pl 2>/dev/null
cp -p $CYT_DIR/Scripts/IndxImg.txt $CYTW_DIR/Collab
ls -l $CYTW_DIR/Collab/IndxImg.txt
# ----------------------------------------------------------
### indexation of PMID
echo "Indexation of PMID"
perl $CYT_DIR/Scripts/parsing_med.pl 2>/dev/null
## indexation of bibliographic references
echo "indexation of bibliographic references"
perl $CYT_DIR/Scripts/parsing_ref.pl 2/dev/null > ../../chromcancer/Collab/url_ref.txt
ls -l ../../chromcancer/Collab/url_ref.txt
## indexation of bibliographic references
echo "indexation of bibliographic references"
perl $CYT_DIR/Scripts/parsing_biblio.pl 2>/dev/null > ../../chromcancer/Collab/parsing_biblio.txt
ls -l ../../chromcancer/Collab/parsing_biblio.txt
# ----------------------------------------------------------
cd $CYT_DIR/Scripts
echo "copies dans ../../chromcancer/Collab"
# copies in ../../chromcancer/Collab
## copy des ObjDB.txt   dans $CYTW_DIR/Collab/
cp -p ObjDB*.txt $CYTW_DIR/Collab
## copy of ObjDB1.html   in $CYTW_DIR/Collab/
mv ObjDB*.html $CYTW_DIR/Collab
## copy of GeneExtlnk.txt in $CYTW_DIR/Collab/
mv GeneExtlnk.txt $CYTW_DIR/Collab
mv GeneExtlnk.html $CYTW_DIR/Collab
##mv $CYT_DIR/Scripts/GeneLink.txt $CYTW_DIR/Collab
## copy of cytoentities.html
## copie of tabulated files : forsale et catalog
cp forsale_out.txt $CYTW_DIR/Collab
cp catalog_out.txt $CYTW_DIR/Collab
cp forsale $CYTW_DIR/Collab
cp catalog $CYTW_DIR/Collab
cp catalog_full.txt $CYTW_DIR/Collab
## copie du fichier genes_cancer.txt
cp -p genes_gc.txt $CYTW_DIR/Collab
cp -p genes_gn.txt $CYTW_DIR/Collab
cp -p genes_gcr.txt $CYTW_DIR/Collab
## copy of genes non_cancer
cp -p genes_gn.txt $CYTW_DIR/Collab
# copy of parsing_med
cp -p list_refmedline.txt   $CYTW_DIR/Collab
#
chmod 664 $CYTW_DIR/Collab/*.txt
chmod 664 $CYTW_DIR/Collab/*.html
# ----------------------------------------------------------
# generation of the genes atlas file
echo "Generation du fichier gene_atlas.txt "
filtcol genes_gc.txt 45 "<>" "-" > $CYTW_DIR/Collab/genes_atlas.txt
ls -l $CYTW_DIR/Collab/genes_atlas.txt
# ----------------------------------------------------------
# generation of the humprot_atlas.txt file
prtab $CYTW_DIR/Collab/genes_atlas.txt 1 2 10-12 22-23 46 > $CYTW_DIR/Collab/humprot_atlas.txt
echo "generation of the humprot_atlas.txt file"
ls -l $CYTW_DIR/Collab/humprot_atlas.txt
# ----------------------------------------------------------
## copy of Amplicons
echo "copy of amplicons"
cp -p $CYT_DIR/Ampl/*.html   $CYTW_DIR/Ampl
cp -p $CYT_DIR/Ampl/Images/*.jpg   $CYTW_DIR/Ampl/Images
# ----------------------------------------------------------
# Categories
# indexation of images
cd $CYT_DIR/Scripts
echo "indexation of categories "
cd $CYT_DIR/Scripts/Data/Category_editor
./prepcat2.sh
cd $CYT_DIR/Scripts
$CYT_DIR/Scripts/indximgcategory.pl 2>/dev/null
$CYT_DIR/Scripts/index_category2.pl 2>/dev/null
ls -l Categories_img.txt
ls -l category_img.txt
ls -l category_lst.txt
cp -p catdeepgene.txt    $CYTW_DIR/Collab/catdeepgene.txt
cp -p Categories_img.txt $CYTW_DIR/Collab/Categories_img.txt
cp -p category_img.txt   $CYTW_DIR/Collab/
cp -p category_lst.txt   $CYTW_DIR/Collab/
# ----------------------------------------------------------
# generation of atlas_statuts
perl $CYT_DIR/Scripts/atlas_status.pl 2> /dev/null
echo "rebuild of Status directories"
ls -l $CYTW_DIR/Status/Status_*html
# ----------------------------------------------------------
# Indexation of ICD
perl $CYT_DIR/Scripts/index_icd_topo.pl 2> /dev/null
perl $CYT_DIR/Scripts/index_icd_morph.pl 2> /dev/null
# ----------------------------------------------------------
# Update of recents files (2 years)
echo "Update of recents files (2 years) "
# lastfiles : Report.html
$CYT_DIR/Scripts/lastfile.pl 2>/dev/null
ls -l $CYTW_DIR/Recent.html
# ----------------------------------------------------------
# Statfiches
echo "statfiches "
$CYT_DIR/Scripts/statfiches.pl 2>/dev/null
ls -l $CYTW_DIR/Collab/StatFiches.html
# ----------------------------------------------------------
# Update of Backpage
# modifBackpage creates a Backpage2.html file
# the addlist file contains new authors
#$CYT_DIR/Scripts/modifBackpage addlist
#cp $CYTW_DIR/BackpageAbout.html $CYTW_DIR/BackpageAbout0.html #mv $CYTW_DIR/BackpageAbout2.html $CYTW_DIR/BackpageAbout.html
cp $CYT_DIR/Scripts/listeAuthBPage.txt $CYTW_DIR/Collab/
# ----------------------------------------------------------
# creation of a synthesis file JLH ObjDB6.txt
echo "creation of ObjDB6.txt "
majfich4.pl 2>/dev/null
ls -l $CYTW_DIR/Collab/ObjDB6.txt
# ----------------------------------------------------------
# List of regular updates (depending of releases)
# creation of chromcancer/cosmic_study.html
# read of ../Standards/COSMIC/cosmic_study.txt
./cosmic2html.pl
#
# ICGC : list of projects
# creation of ../../chromcancer/icgc_projects.html
# Lecture de ../TCGA_ICGC/ICGC/cgc_projects.txt
./icgc2html.pl
#
# copies of the Band files
cp $CYT_DIR/Scripts/tmp_allgenes.txt $CYTW_DIR/Collab
cp $CYT_DIR/Scripts/tmp_allanom.txt $CYTW_DIR/Collab
cp $CYT_DIR/Scripts/anom_bandall.txt $CYTW_DIR/Collab
cp $CYT_DIR/Scripts/gene_bandall.txt $CYTW_DIR/Collab
# list of files on archive ( Collab )
echo "list of files on archive $CYTW/Collab "
ls -lt $CYTW_DIR/Collab
# Update of the data on index.html
# Sun Aug 12 12:09:46 MEST 2007
# Sat Nov 21 10:28:10 MET 2009
# Thu Jul 9 15:36:42 MEST 2015
DATEOUT=`date`
# to be adapted to time/date format (depending of UNIX)
perl -pi.bak -ne 's@\S+ \S+ \d+ \d+:\d+:\d+ MEST 20\d\d@$DATEOUT@' $CYTW_DIR/index.html
rm $CYTW_DIR/index.html.bak
echo "start of indexation $DATEIN"
echo "end of indexation   $DATEOUT"
# ----------------------------------------------------------
# statistics
$CYT_DIR/Scripts/stat_atlas.pl > $CYTW_DIR/stat_atlas.html
#
echo "Do not forgot to update the key_date_pays.txt file"
ls -l key_date_pays.txt
# Update of the MySQL indexation (only on INIST)
# ----------------------------------------------------------
############################################################

Atlas website structure

2017-07-25T08:39:29+02:00

The Atlas website structure
http://atlasgeneticsoncology.org
Philippe Dessen (Database Director) dessen@igr.fr
Jean Loup Huret (Editor) jean-loup.huret@atlasgeneticsoncology.org
May 2018

I- Main page:

II-1.

Foreword 1: There are various types of items developed in the Atlas:
1- Genes (http://atlasgeneticsoncology.org/Genes/XXX )
1-1. Annotated genes (papers/cards written by authors) URLs: http://atlasgeneticsoncology.org/Genes/[name-of-gene]ID[number]ch[location].html (1,493 papers/cards, e.g. http://atlasgeneticsoncology.org/Genes/PGRID41700ch11q22.html); and
1-2. Automated cards on genes (more or less like GeneCards); URLs: http://atlasgeneticsoncology.org/Genes/GC_[name-of-gene].html (28,377 cards);
2- Leukemias 681 annotated papers/cards : http://atlasgeneticsoncology.org/Anomalies/XXX , and 540 "Other Leukemias" (automated cards) : http://atlasgeneticsoncology.org/Anomalies/TL_XXX .
3- Solid tumors 217 annotated papers/card : http://atlasgeneticsoncology.org/Tumors/XXX , and 2,968 "Other Tumors" (automated cards) : http://atlasgeneticsoncology.org/Tumors/TT_XXX .
4- Cancer-prone diseases 114 annotated papers/cards : http://atlasgeneticsoncology.org/Kprones/XXX .
5- Case reports in hematology (http://atlasgeneticsoncology.org/Reports/XXX ) (88 papers/cards)

All these cards are structured from templates (e.g. Submission form for GENES: http://atlasgeneticsoncology.org/Forms/Gene_Form_for_submission.doc) with the addition of a HEADER with tags or tracking devices allowing for indexing of the form in different parts of the data base (e.g. TRI_PAR_CHROMOSOME -> to which chromosome page (red arrow)? CATEGORY-> to which Cell Biology page (red arrow)?); see also: http://atlasgeneticsoncology.org/Collab/catalog and http://chromosomesincancer.org/en/template-for-cards-papers.html ;
- and EXTERNAL LINKS (bottom of each paper/card).
There are also
- Deep Insights (traditional papers) http://atlasgeneticsoncology.org/Deep/XXX (113 Deep)
- Chromosome pages (http://atlasgeneticsoncology.org/Indexbychrom/idxa_[chromosome-number].html e.g. http://atlasgeneticsoncology.org/Indexbychrom/idxa_11.html ) and
- Chromosome band pages (http://atlasgeneticsoncology.org/Bands/[band].html e.g. http://atlasgeneticsoncology.org/Bands/19p13.html ),
- Cell biology pages (http://atlasgeneticsoncology.org/Categories/[category-name] e.g. http://atlasgeneticsoncology.org/Categories/Cell_cycle.html
- ICD-O pages (International Classification of Diseases - Oncology WHO/OMS) e.g. http://atlasgeneticsoncology.org/Tumors/Solid_Nosology.html and http://atlasgeneticsoncology.org/ICD/icd_2016_topo.html
- Atlas status (thesaurus of the Atlas: http://atlasgeneticsoncology.org/Status/Status.html and sub-pages)
- and various other pages (Backpage: http://atlasgeneticsoncology.org/BackpageAbout.html Recent papers http://atlasgeneticsoncology.org/Recent.html , Educational items http://atlasgeneticsoncology.org/GeneticEng.html , Genes partners, International cancer programs etc. (see others on the Main page)

A. Architecture of data:
A1. Text files for cards
Genes0
Anomalies (Leukemias)
Tumors
Kprones (Cancer-prone hereditary diseases)
Reports (Case Reports)
Deep (Deep Insight)
Educ (Educational Items)
The 2 last are defined by a couple of files (.meta + .htm)
A2. Chromosomal location
at the chromosome level
at the chomosomal band level
A3. Functional categories (Cell Biology)
A4 Count/Census of Atlas Items
Statistics on atlas files, see: http://atlasgeneticsoncology.org/Status/Status.html , and http://atlasgeneticsoncology.org/stat_atlas.html
A5. Catalogs and indexes
see in http://atlasgeneticsoncology.org/Collab/
catalog_full.txt (tabulated file with major informations from HEADER and IDENTITY blocs)
ObjDB0.txt ObjDB2.txt ObjDB4.txt ObjDB6.txt ObjDB.txt
ObjDB1.txt ObjDB3.txt ObjDB5.txt ObjDB7.txt: different files for indexing (might be simplified in a new structure)
A6. External resources

B. Modules for management and development
Module 1: Description of the templates of cards
see: http://atlasgeneticsoncology.org/Collab/Formes.xlsx ,
which correspond to the various submission forms for the authors:
http://atlasgeneticsoncology.org/Forms/Gene_Form_for_submission.doc
http://atlasgeneticsoncology.org/Forms/Leukemia_Form_for_submission.doc
http://atlasgeneticsoncology.org/Forms/Solid_Tumor_Form_for_submission.doc
http://atlasgeneticsoncology.org/Forms/Cancer-Prone_Disease_Form_for_submission.doc

Each card has a unique Atlas ID (present in the filename)
Genes: 1 --> 999 + 40000 --> 80000
Anomalies: 1001 --> 4999
Tumors: 5000 --> 9999
Kprones: 10000 --> 19999
Deep: 20000 --> 29999
Educ: 30000 --> 3999

Organisation of directories
All data is organized in two main directories
1. "cytatlas" (for managment)
2. " chromcancer" (with internet access)

1. cytatlas
./Genes0 (for expert txt)
./Genes (after txt processing)
./Anomalies
./Tumors
./Kprones
./Reports
./Deep
./Educ
Each directory has some other subdirectories for Images, xxLinks …
./Scripts (all bash and perl + references data)

2. chromcancer
./Genes
./Anomalies
./Tumors
./Kprones
./Reports
./Deep
./Educ
(each of the above with subdirectories for Images ..)
./Categories
./Indexbychrom (Chromosomes pages)
./Indexbyalpha
./Bands
./Status
./ICD
./ISCN

The process of scripts is in general made in the ./cytatlas/Scripts
The directory can be installed in a way defined by a general shell script
Cytatlas.sh which defines all the logical variables.

#!/usr/bin/bash
## script cytatlas_cygwin disque D
umask 002
CYT_DIR='/cygdrive/d/ATLAS/cytatlas'
CYTW_DIR='/cygdrive/d/ATLAS/chromcancer'
CYTHTML_DIR='http://genome.igr.fr/chromcancer'
SCRIPT_DIR='$CYT_DIR/Scripts'
PATH=$PATH:$CYT_DIR/Scripts
export CYT_DIR CYTW_DIR CYTHTML_DIR SCRIPT_DIR PATH

GENE_DIR=$CYT_DIR/Genes
ANOM_DIR=$CYT_DIR/Anomalies
TUMOR_DIR=$CYT_DIR/Tumors
KPRON_DIR=$CYT_DIR/Kprones
REPORT_DIR=$CYT_DIR/Reports
STUDY_DIR=$CYT_DIR/StudyGroup
DEEP_DIR=$CYT_DIR/Deep
EDUC_DIR=$HOME/DATA_DIR/Educ
WGENE_DIR=$CYTW_DIR/Genes
WANOM_DIR=$CYTW_DIR/Anomalies
WTUMOR_DIR=$CYTW_DIR/Tumors
WKPRON_DIR=$CYTW_DIR/Kprones
WREPORT_DIR=$CYTW_DIR/Reports
WDEEP_DIR=$CYTW_DIR/Deep
WEDUC_DIR=$CYTW_DIR/Educ
WCOLLAB_DIR=$CYTW_DIR/Collab
export GENE_DIR ANOM_DIR TUMOR_DIR KPRON_DIR
export REPORT_DIR STUDY_DIR DEEP_DIR EDUC_DIR
export WGENE_DIR WANOM_DIR WTUMOR_DIR WKPRON_DIR
export WREPORT_DIR WDEEP_DIR WEDUC_DIR WCOLLAB_DIR

alias cyt='cd $CYT_DIR'
alias cytw='cd $CYTW_DIR'
alias cyti='cd $CYT_DIR/Scripts'
echo 'cyt : $CYT_DIR'
echo 'cyti : $CYT_DIR/Scripts'
echo 'cytw : $CYTW_DIR'
echo 'www : $CYTHTML_DIR'

Module 2: Editorial management of cards
Foreword 2: Editorial process:
This is an important part, as the Editorial database processing must take it into account. See "Editorial workflow in the Atlas": http://chromosomesincancer.org/en/editorial-workflow.html .
In particular, critically important, Tables are used 1- to identify all/each relevant item (Table 1 herein below); 2- to dialogue with authors (Table 2).
These tables are the today ones used by the editor.
Examples:

NAME	STATUS	AUTHORS	ID Atlas	ICD-O3_MORPH	ICD-O3_TOPO
05;00§ tri 5/NHL or chronic Lympho	FOR SALE				C421,C424
05;00§ MDS with isolated del (5q)	DONE	XX	1134	9986/3	C421,C424
05;00§ del(5)(q32q33) TNIP1/PDGFRB	Reserved	XXXX	1773		C421,C424
… about 1,000 items/lines
99;99§ Extraosseous plasmacytoma	Reserved	XXXXXX	1718	734/3	C421,C424
99;99§ Florid follicular hyperplasia PTLD	Reserved	XXX	1788		C421,C424

AUTHOR	e-mail	"Translocation"	DEADLINE	COMMENTS
XXX	XXX@xx	Florid follicular hyperplasia PTLD	DONE	3rd paper (leuk.) + 1 paper (gene)
XXXX	XXXX@xxxx	del(5)(q32q33) TNIP1/PDGFRB	?????	Reminder 2017/06/26; 2017/03/21"Yes, will have this to you shortly"; Reminder 2016/11/19; Reminder 2016/06/17; 2016/01/17 no deadline ("soon"); 2015/10/14: OK
XXXXX	XXXXX@xxxx	del(X)(p22p22) (P2RY8/CRLF2)	16/03/2017	Spontaneous proposal

Note: Tables used to identify all/each relevant item must be related (bijective type relation) with cards/papers; e.g. 05;00§ MDS with isolated del (5q) / ID 1134 <--> http://atlasgeneticsoncology.org/Anomalies/del5qSoleID1134.html

These tables may not exist per se. They would be integrated in the database of the Atlas (as, so far, some files as catalog, authors lists … on the INIST server. and automatically generated. But the right way will be to use ONLY screens developed ad hoc for editorial management.

Finally, we also have to format the cards/papers into word for the "scientific journal" version (see http://documents.irevues.inist.fr/handle/2042/15655 (e.g. http://documents.irevues.inist.fr/bitstream/handle/2042/62324/10-2014-HSPD1ID40888ch2q33.pdf , equivalent of http://atlasgeneticsoncology.org//Genes/HSPD1ID40888ch2q33.html ) of the Atlas.
A module is being finalized concerning the production of the scientific journal: It is a Web application developed with PHPWord/MySQL/Symfony Framework.

2.1 Actual process of management:
• Reception of a doc file (structured in the ad hoc template.
• Edition in a text file with good fields (validate the presence of a field in the beginning of lines (with eventually multiplicity of the same field)
• Addition of internal links (an expert task)

• Complementary procedure (by scripts)
- Correction of special characters (non compatibility between office Word and hypertext)
- Validation of bibliography with dowloading the short description of PubMed with PMID.
- Reordering biblio with alphabetic order
- Tests of good fields for each line (in good blocs)
- Test of links ( existent Atlas ID).
- Test of logical structure of each bloc (BEGIN.. / END)
- Transformation in hypertext documents (see further)

2.2 To be developed for a new management:
- On-line templates must be available to the authors who will write directly their paper (e.g. http://atlasgeneticsoncology.org/Forms/Gene_Form_for_submission.doc , corresponding to http://chromosomesincancer.org/en/atlas-templates-for-cards.html ). These templates must be capable of evolution when the Editor(s) in Chief wish to add or delete or modify a tag or even a "BEGIN_END". A password would allow the author to interrupt his writing, save, and come back latter until a last validation.
- A macro-instruction assisting the recognition of an internal hyperlink that the editorial staff member must add before publishing (e.g. ABL: a list of "NAMES" and aliases must help to recognize and propose the hyperlink to ABL1; the editorial member says OK, and the hyperlink to http://atlasgeneticsoncology.org/Genes/ABLID1.html comes automatically): --> need of a thesaurus (e.g. http://atlasgeneticsoncology.org/Tumors/Solid_Nosology.html
- PMID numbers solely permits to give the full reference
- Special characters are automatically transcribed (e.g. https://text-symbols.com/html/entities-and-descriptions , http://www.symbole-clavier.com , http://alexandre.alapetite.fr/doc-alex/alx_special.html ).

Module 3: Indexations
All the files of Atlas are considered as "objects" and are defined by an Atlas ID.
The standard of the filename of the objects is the following:
- Genes: 2 forms:
<String>ID<number><location>.txt Ex: ADCYAP1ID43656ch18p11.txt
<String>ID<number>.txt Ex: AF6ID6.txt
A generic form is built fr an easy links. The filename id defined as:
GC_<symbol>.txt e.g.: GC_ZFP90.txt
- Anomalies (Leukemias)
- Tumors
- Kprones
The filename is as : <string>ID<number>.txt ( ex :t3q21q26TreatRelLeukID1236.txt)
Creation (or Updating) of index or cards
As mentioned in the indexation.sh script (the main indexation performed after some modifications)
Indexation of Cards 1: script indexation.sh (in cytatlas/Scripts)
Used for re-indexation after new files or new data
http://atlasgeneticsoncology.org/Collab/Scripts/indexation.sh
1. Generation of all automatic genes
2. Generation of the main index file for all documents (ObjDB.txt)
3. Generation of some others indexes (ObjDBxx.txt ) (see in http://atlasgeneticsoncology.org/Collab/)
- ObjDB.txt
- ObjDB0.txt
- ObjDB1.html
- ObjDB1.txt
- ObjDB2.txt
- ObjDB3.txt
- ObjDB4.txt
- ObjDB5.txt
- ObjDB6.txt
- ObjDB7.txt
4. Generation of a catalog (text file with the information from the HEADER, see: http://atlasgeneticsoncology.org/Collab/catalog)
5. Transformation of the catalog (and "for sale" - "to be written" files) in tables with concatenation in a catalog_full.txt file)
6. Indexations of Genes (Geneliste.html), Leukemias (Anomliste.html), etc.
7. Indexation by chromosomes
8. Indexation by authors (different IndxAuthxx.txt / html in Collab) (IndxAuth3.txt is the main index for authors and affiliations)
9. Generation of Categories (several files are maintained before in parallel) for Cell Biology items
10. Generation of status (Genes .. Authors . etc.): http://atlasgeneticsoncology.org/Status/Status.html
11. Generation of Recent (last 2 years documents): http://atlasgeneticsoncology.org/Recent.html
12. Generation of COSMIC projects and TCGA/ICGC projets
13. Statistics (http://atlasgeneticsoncology.org/stat_atlas.html)
Possibility of mysql indexation for some items (query in the home page)

Module 4: Internal cross links between classes of cards
This section is important and gives a plus at the Atlas with numerous additions of links between cards. These links (Gene -> tumors, Leukemia <- genes …) enrich the quality and the expertise of the Atlas.
An automatic procedure parses all the cards and indexes the location of links (defined as a standard by the pattern ( <: TXT: text ID: AtlasID).
http://atlasgeneticsoncology.org/Collab/Scripts/maj_full.sh
This script has 2 goals: definition of all internal links
and
Generation of all hypertext files (readable on the net)

Map of one set towards another: injectivity/surjectivity:

Item	Internal hyperlink toward
1 Gene	n1 Leukemias
	n2 Solid tumors
	n3 Cancer-prone

1 Leukemia	n4 Genes
	n5 Cancer-prone

1 Solid tumor	n6 Genes
	n7 Cancer-prone

1 Cancer-prone	n8 Genes
	n9 Leukemias n10 Solid tumors

Examples:

Item		Hyperlinks toward
Gene	NUP214	Leukemia	t(6;9)(p23;q34) DEK/NUP214
		Leukemia	t(9;9)(q34;q34) SET/NUP214
		Leukemia	T cell ALL
		Solid Tumor	Lung Adenocar. t(9;9)(q34;q34) PRRC2B/NUP214

Gene	KIT	Leukemia	trisomy 4
		Solid Tumor	Melanoma
		Cancer Prone	Piebaldism

Leukemia	t(6;9)(p23;q34) DEK/NUP214	Gene	NUP214
		Gene	DEK

Cancer Prone	Tuberous sclerosis	Gene	TSC1
		Gene	TSC2
		Solid Tumor	Renal carcinoma
		Solid Tumor	Ependymomas

Module 5: Management of external links
Files for annotation of genes:
A parallel management of several databases is regularly made (from NCBI, UCSC, UniProt, Ensembl, HGNC, COSMIC, Mitelman (NCI) …)
All genes defined in the Atlas are based of the update list of gene symbols of human Entrez_genes . A great part of annotations are also associated ones in the ftp files of (ftp.ncbi.nih.gov/gene/DATA/ and /gene/GeneRIF). They are managed by script to lead in 2 tabulated files (genes_gc.txt and genes_gn.txt ) , the first one for « cancer genes » (some words in description and/or GeneRif in Entrez Gene),
the second for other genes of Entrez_Gene (NCBI). Genes used are limited to a genome location (hg38) defined in http://hgdownload.soe.ucsc.edu/goldenPath/hg38/database/refGene.txt.gz.
See: for a definition of all the fields keep updated and used in External links of the cards on Genes: External_annotations_genes

Module 6: Statistics
- Topics/Items for the Atlas (genes, leukemias, solid tumors and others):
- Need of Tables (e.g. http://atlasgeneticsoncology.org/Collab/ID-TRANSLOC.txt ) to know what is done, what is done but old, what is reserved to a given author, what needs an author to be found. Allows the addition of new items.

Atlas Users

2015-12-18T13:50:51+01:00

USERS of the

Atlas of Genetics and Cytogenetics in Oncology and Haematology

http://AtlasGeneticsOncology.org

There are many random visits, as is usual with internet queries; on the other hand we are aware that many professionals (such as cytogeneticists) prefer to enter a keyword directly on Google, such as "t(9;22)(q34;q11)" than passing through the home page of the Atlas, which introduces a bias the other way: a query from a robot may also come from a frequent/professional user.

However:

1. There are regular users, from University and/or Hospital cities.

2. Many users are from academic sites.

3. A number of private companies also use the Atlas.

4. The Atlas has an international audience, not only in rich countries, but also in emerging countries.

- 5,500 unique visits every day

- 1.5 million visits a year

- 25% from the USA,

- but also frequent use from emerging countries

Figure 1 Regular users are our real core target (Cytogeneticists, Hematologists, Researchers, University Teachers).

Figure 2 Geographical Origin: dominance of the USA

Figure 3 Consultation in North America centered on university and/or medical areas: New York, Houston, Chicago, Los Angeles, Boston, San Diego, Salt Lake City, Montréal, Philadelphia, Toronto …

Figure 4 Consultation in Western Europe:Paris, Lyon, Munich, Toulouse, Brussels, Lille, Berlin, Vienna, Montpellier, Zurich, Nantes …

Figure 5 Consultation in Northern Europe: London, Dublin, Glasgow, Sheffield, Edinburgh, Oxford, Helsinki, Stockholm, Cambridge, Copenhagen …

Figure 6 Consultation in Southern Europe: Madrid, Milano, Roma, Barcelona, Napoli, Valencia, Seville, Athens, Turin, Lisbon …

Figure 7 Consultation in Southern America: Bogota, Santiago, Buenos-Aires, Quito, La Victoria, Medellin, Caracas, Cali, Sao Paulo, Barranquilla …

Figure 8 Consultation in South Asia: New Delhi, Bengaluru, Mumbai, Chennai, Hyderabad, Kolkata, Pune, Tehran, Lahore, Karachi …

Figure 9 Consultation in Eastern Asia: Seoul, Hong Kong, Beijing, Shanghai, Wuhan, Gyeonggi-do, Osaka, Busan, Minato, Kyoto …Quezon, Bangkok, Singapore, Kuala Lumpur, Selangor, Manila, Makati, Cebu City, Ho Chi Minh, Jakarta …

Figure 10 Consultation in Africa: Tunis, Casablanca, Cairo, Algiers, Lagos, Cape Town, Rabat, Dakar, Alexandria, Johannesburg …

Figure 11 Consultation in Australasia: Sydney, Melbourne, Brisbane, Perth, Adelaide, Auckland, Canberra, Wellington, Newcastle, Christchurch …

Argument

2015-12-18T09:51:21+01:00

Project title

'Atlas of Genetics and Cytogenetics in Oncology and Haematology'

internet journal / encyclopaedia /database http://AtlasGeneticsOncology.org

Summary

The Atlas is a peer reviewed internet journal / encyclopaedia / database devoted to:

- genes implicated in cancer,

- cytogenetic or clinical entities in cancer, and

- hereditary diseases which are cancer-prone conditions.

Size of the Atlas in 2015: number of pages: 45,500; 3,500 authors; 5,500 visits every open day; 1,1 million unique user every year (USA 27%).

Key words

- Pooling of knowledge concerning the biology of normal and cancerous cells,

- Referential and investigation tool for research,

- Multilingual pedagogical support,

- Translational health research

- Transfer of scientific innovation towards research itself, and, downstream, towards patient care

Context

25,000 new publications concerning cancer genetics in man are added each year in PubMed. No one, anymore, has the whole required knowledge, necessary to guide the treatment procedure in case of a rare disease. Huge database are therefore needed, to collect and summarize data on these rare diseases, and produce meta-analyses.

Objectifves of the project

- Medical treatment assistance in rare forms of cancer,

- Efficiency savings in the fight against cancer,

- Decrease in fundamental and applied research as well as medical costs.

- Personalised medicine for cancer (one of the axes of the cancer plans).

I- Scientific Background

General description / relevance and originality of the project Prognosis of a leukaemia depends on the genes involved: 5 years survival: 6% in the inv(3)(q21q26) RPN1/MECOM leukemia, 100% in the dic(9;12)(p13;p13) PAX5/ETV6 leukemia. And treatments, indeed, depend on the severity of the disease. However, 2,000 to 9,000 genes are possibly implicated in cancer, and 1,200 types of solid tumours exist. Some cancers are frequent while many others are very rare (only 1 published case), this is particularly true for leukemias subtypes … but there are more than 900 leukemias!No one, anymore, has the whole required knowledge, necessary to guide the treatment procedure in case of a rare disease. Huge database are therefore needed, to collect and summarize data on these rare diseases, and produce meta-analyses. L’ Atlas contributes to 'meta-medicine', this mediation between the knowledge and the knowledge users in medicine.

II- International positioning of our team / Current organization

The Atlas is one of the pioneers of the Internet, it started in 1997. It meant writing short cards on genes and chromosomes implicated in cancer. The Atlas is now 45,500 pages big, written by more than 3,500 authors, from about 50 countries (France, USA, Italy, United Kingdom, Germany, Japan, Spain, Canada, China, The Netherlands ...).

The Atlas is in free access, which is particularly useful for third world countries or for students.

- Topic research The Atlas participates in research on cancer epidemiology. The Atlas is a tool in genomic studies of the latest generation (see Science 28 Jan 2011, vol 331 p 435-439, suppl data, where the authors indicate that they have used the Atlas and Cosmic as reference databases to choose and test a series of genes in medulloblastoma in childhood). Nonetheless, the Atlas' aim is not to overlap with the databases daily used in molecular biology (UCSC, Ensembl, Entrez, Cosmic, Swiss-Prot). However, as these data are in the public domain, we could easily produce them, according to the needs of the community.

- Topic teaching and continuing medical education The Atlas is at the crossroads of research, university and post-university teaching (virtual medical university) and telemedicine.

- Database on genes: Where else can be found so many detailed articles on genes? see: PTN or BCL6 http://atlasgeneticsoncology.org//Genes/PTNID41904ch7q33.html and http://atlasgeneticsoncology.org/Genes/BCL6ID20.html.

- Electronic journal version of the Atlas An Open access electronic journal /pdf version of the Atlas is being developed by Institute for Scientific and Technical Information (INIST) of the French National Centre for Scientific Research (CNRS). Available are the archives of a quarterly journal since 1997, which became a bimonthly journal in 2008 and a monthly journal in 2009, comprising 2,500 articles in more than 120 volumes, which constitutes a 10,000 pages collection, available at: http://irevues.inist.fr/atlasgeneticsoncology, allowing the Atlas, soon, to be referenced by the main bio-medical databases, including PubMed.

- The Atlas combines various types of knowledge all on one site: Genes and their function, cell biology, diseases, cytogenetics, but also clinical genetics, including hereditary diseases which are cancer-prone conditions. This tends to unify cancer genetics, while data are elsewhere dispersed between several sites[1]. The iconography in the Atlas is diverse (medical imaging, pathology, chromosomes, 3-D structure of proteins, genetic maps...), which is not found in other sites (apart from genetic maps that can be found in GeneBank, Ensembl …). The Atlas is the only site devoted to genetics where the prognosis is quoted: It has always seemed surprising to us that such a crucial data is just ignored in other sites. There are more than 17,000 internal hyperlinks in the Atlas.

- Diagnosis assistance and information-based therapeutic decision The Atlas contributes to the cytogenetic diagnosis and may guide treatment decision making, particularly regarding rare diseases (because they are numerous, rare diseases are frequently encountered).

- Developments in cell biology and physio-pathology: data in the Atlas are a definite resource in cell biology and physio-pathology, that we are just beginning to harness (e.g.: Apoptosis: http://atlasgeneticsoncology.org/Categories/Apoptosis.html ).

- Towards a personalized medicine of cancer: From our section "Genes", can be extracted 613 genes implicated in colorectal cancer, 750 in breast cancer, and 494 genes in prostate cancer (see paragraph "Other genes implicated " at: http://atlasgeneticsoncology.org/Tumors/breastID5018#EXTRACTED). With the fast development of technics in genetics, it now emerges that many subtypes of solid tumors may exist, following the leukemia model (how many hundreds of breast cancer subtypes, defined by distinct genetic profiles, to be uncovered?). Recently, new data on lung adenocarcinoma made possible to consider personalized medicine (see http://atlasgeneticsoncology.org/Tumors/TranslocLungAdenocarcID6751.html ). This, together with cell biology developments in the Atlas demonstrates that the encyclopedic content is potentially a basis for developing personalized medicine for cancer. It remains to present this knowledge in such an affordable manner that the Atlas truly becomes a tool for the staff meetings.

Renown Prestigious journals, such as Science and Nature Reviews Cancer, have written about the Atlas The Atlas is regularly cited as a journal in leading scientific publications (Annual Review of Biochemistry (Impact Factor 29,88), Science (29,75), Nature Reviews Cancer (29,54), Cancer Cell (25,29), Nature Cell Biology (19,53), Journal of the National Cancer Institute (14,07), American Journal of Human Genetics (12,30), Molecular Systems Biology (12,13), Genes and Development (12,08), Genome Research (11,34), Trends in Molecular Medicine (11,05), Blood (10,56), PNAS (9,43)...). The Atlas is also cited as a reference database in Science. Hyperlinks towards the Atlas have been developed by the National Cancer Institute USA, Swiss-Prot, GeneCards, the Sanger Institute, Mitelman database au NCI, etc... Renown of the Atlas may be checked at: http://chromosomesincancer.org/en/jce/acknoledgements-to-the-atlas.html (Felix Mitelman wrote that the Atlas "has grown into a truly monumental encyclopaedic work of great importance to cancer research (...) an invaluable reference and resource for scientists and clinicians").

Who uses the Atlas?The Atlas is accessed by: 1- Research: cytogenetics, molecular biology, cell biology researchers; 2- Hospital: clinicians, haematologists, cytogeneticists, pathologists, from the teaching hospitals, indeed, but also from general hospitals where the Atlas is one of the rare free resources. Junior doctors in haematology or oncology, are also most receptive to the Atlas that they see as a training and educational tool; 3-Students.

The Atlas receives more than 1,100,000 visits every year (25% of the visitors are from the USA, 12% from France, but many other visitors are from the developing countries. 200 cytogenetic labs come every day, 1,000 visitors more than once a week (cytogenetic labs./university teachers-researchers), and 6,000 visitors more than once a month (university teachers - researchers, students, staff meetings on blood malignancies). 5,500 individual machines connect to us every day. A bug, on May the 23rd, 2008, was devastating: pages on chromosomes, with their data, had vanished; many mails were sent to us, proving that the Atlas was (is) indispensable; see: http://chromosomesincancer.org/en/jce/acknoledgements-to-the-atlas.html#Incident ). See also recent testimonies at :http://atlasgeneticsoncology.org/Supporting_Atlas_First_signatories.pdf

The Atlas is also operated by various biotech and pharma to implement their internal systems and databases.

Comparison with the Mitelman Databasethe Atlas is certainly not redundant with the "Mitelman". As a matter of fact, the Mitelman and the Atlas are complementary: the Mitelman is exhaustive but gives rough data, with no annotation, while the Atlas presents a meta-analysis of the data, giving an overview on a given disease, describing the main clinical characteristics, with, when possible, an iconography of chromosomes (e.g. see: t(1;11)(p32;q23) in each of the two sites).

Scientific societies have decided to grant the Atlas, they thus give a scientific credibility and a clear and real will to the Atlas sustainability and perennialty: Association des Cytogénéticiens de Langue Française et Groupe Francophone de Cytogénétique Hématologique, Belgian Society of Human Genetics et Belgian Cytogenetics Group in Haematology and Oncology, Dutch working group of Tumor Cytogenetics, Berufsverband Deutscher Humangenetiker e.V. et Gesellschaft für Humangenetik e.V., Societa Italiana di Genetica Umana, Grupo Cooperativo Español de Citogenética hematológica and Sociedad Española de Hematología y Hemoterapia, Australasian Society of Cytogenetics.

Structure of the board of the Atlas

- Jean-Loup Huret, associate professor and consultant, CHU Poitiers, editor in chief and Philippe Dessen, research director, CNRS-Institut Gustave Roussy, database director;

- Because, historically, the project could not have been supported by institutional players, a non-profit association (french law 1901) was created (see http://chromosomesincancer.org/en/ ) (president Jean-Loup Huret, geneticist, vice president Hossein Mossafa, geneticist, treasurer Bernard Drochon, external auditor, secretary Martine Jammet, entrepreneur, all volunteers). This association have employed 5 to 6 MSc or PhD co-workers (the main area of expenditure: 30,000 Euro (salary + charges) for each collaborator, but they make an indispensable work -since the Atlas is much more an encyclopedia than a database, requesting a good amount of expertise). The association comprises about 60 members (50% french, 25% americans).

- A scientific committee of the association (http://chromosomesincancer.org/fr/jce/conseil-scientifique.html ), including delegates from various scientific societies; and there is also an editorial board for the Atlas (http://atlasgeneticsoncology.org/Backpage.html#EDITORIAL ).

III- Development steps

To reach its principal object -the patient service-, the Atlas must become "clinic orientated". To encourage the clinical physician to use the Atlas in his decision making, the Atlas must provide the required information, and such in a "clinician friendly" manner.

A part of our activity must be dedicated to bioinformatics developments, at a time when new fields of cytogenetic are developing with the massive use of FISH, CGH, exome and genome sequencing. Numerous and precise data on mutations, structures variations as well as on gene fusions are taking over the literature.

Adding information with a clinical orientation and into a customized therapeutic care. Developing the knowledge and the scientific innovation transfer into the care system, in particular as part of targeted therapies. Developing decision trees (using the High Authorities recommendations for each pathology); making a list of all the examinations to be performed according to each step of the

Atlas Added Value

2015-12-18T09:21:41+01:00

Added value of the Atlas

Encyclopedia containing original monographs written by different authors, the Atlas combines different types of knowledge. No other web site presents so many monographs on genes, very rich iconography. It is a tool for researchers in genomics, for clinicians as a help in diagnosis and therapeutic decision, for a personalized cancer medicine. The Atlas is not only a web site and an encyclopedia, but also a scientific journal.

In conclusion, it is an original/unique database without equivalent.

Positive aspects of the Atlas

Encyclopedia composed of documents that are original monographs written by invited authors, based on their expertise in a given field (ex: Carlo M Croce on "Common fragile sites and genomic instability", Rolf Marschalek on the KMT2A (MLL) gene, George C Prendergast on the IDO1 and 2 genes, Cécile Badoual on "Head and Neck paragangliomas", Maurizio Genuardi on "MUTYH-associated polyposis", Felix Mitelman on "Cancer Cytogenetics"). Other databases present texts on genes (for example Aceview) but these are non-expertized texts, resulting from data mining. GeneCards is a database with links to other databases, with few data copied from these databases.

Starting first from cytogenetics, the Atlas combines different types of knowledge in a single web site: genes and their function, cell biology (ex: Apoptosis:http://atlasgeneticsoncology.org/Categories/Apoptosis.html), pathological data, diseases and their clinical implications, cytogenetics, but also medical genetics, with hereditary disorders associated with an increased risk of cancer. This gives a wider and more global view of cancer genetics, while these data are usually dispersed[1]. The Atlas is the only genetic site where the prognosis is included; it has always surprised us that data so important such as prognosis could be absent in other sites… even more now in the context of personalized cancer medicine.

No other site, journal or book has so many monographs on genes (more than 1,400 genes; ex:http://atlasgeneticsoncology.org//Recent.html), together with 28,000 non-annotated cards based on the GeneCard type (ex: http://atlasgeneticsoncology.org//Indexbychrom/idxa_11.html, see paragraph on "Other genes").

Very rich iconography on chromosomal aberrations (700 images, ex:http://atlasgeneticsoncology.org/Anomalies/t0609ID1014.html), on genes (3,000 images ex:http://atlasgeneticsoncology.org/Genes/EWSR1ID85.html), on clinics and pathology (400 images, ex:http://atlasgeneticsoncology.org/Tumors/OralMelanomaID6647.html).

Research axis: the Atlas is a tool for researchers in genomics (see Science, 2011). Documents on genes having more and more importance in the analysis of an abnormality, mutations and fusions in relation with NGS: the Atlas is a tool allowing an expert selection of genes involved in cancer. It has been referenced several times as a pertinent source in relation with an abnormality, more particularly as identification of genes associated with the abnormality.

Help in diagnosis and therapeutic decision: the Atlas guides the cytogeneticist by its iconography on chromosomal abnormalities, informs the clinician on rare pathologies, allowing him to adjust his treatment. The Atlas is particularly indispensable in rare diseases (because rare diseases are numerous, these are frequent). All the cytogeneticists from all around the world regularly use the Atlas, as it appeared with recent financial issues[2].

Towards a personalized cancer medicine: 322 genes involved in colon cancer, 457 in breast cancer and 589 in prostate cancer can be extracted from the "gene" section (see paragraph "Other genes implicated"http://atlasgeneticsoncology.org//Tumors/breastID5018.html). With the development of new techniques, it is now evident than solid tumors, as leukemia, have numerous sub-types (how many hundreds of breast cancer with different genetic profiles?). This, added to the development in cell biology, shows that the encyclopedic contents of the Atlas is potentially a basis for the development of personalized cancer medicine.

The Atlas is not only a web site and an encyclopedia, but also a scientific journal. The pdf format of the Atlas (http://irevues.inist.fr/atlasgeneticsoncology) constitutes the archives of a journal published 4 times a year since 1997, then 6 times in 2008, and 12 times in 2009. It includes 2,500 articles in more than 100 volumes, and 9,000 pages to allow us to be referenced by PubMed in the future.

Ergonomy: Access by pages (ex: chromosomeshttp://atlasgeneticsoncology.org/Indexbychrom/idxa_14.html) , by table of anomalies, genes and fusion genes by chromosomal band (ex:http://atlasgeneticsoncology.org/Bands/11q23.html#GENES), with the more recent data on chromosomal abnormalities and fusion genes compiled (TCGA, Cosmic, TicDB, etc.). Synthetic tables (ex: nosologyhttp://atlasgeneticsoncology.org/Tumors/Solid_Nosology.html, patterns, categories, etc.).

The initial structure (independent documents) was improved to allow numerous internal hypertext links: i) direct links and ii) call for links from a given document to a wide range of other documents (ex: tumors associated with a given gene). The Atlas contains more than 17,000 internal links. It is bound to get enriched from its own contents by meta-analysis scripts.

Gestion of external links towards the majority of interesting public databases is automatic.

The Atlas is referenced by other web sites (NextProt, GeneCards, Mitelman database, COSMIC, etc.).

The Atlas benefits from the material support of INIST (CNRS-INSERM), allowing an excellent internet access (more than 1.5 million visits in a year).

In conclusion: original database with no equivalent or concurrence, therefore necessary, besides several other databases, for an in-depth analysis (ex: Atlas + Mitelman + Gene at NCBI + Cosmic).

… However …

Lack of exhaustivity and lack of update of the existing documents (due to lack of staff and the amount of work to be done - the Atlas has already more than 50,000 pages).

Need for the database restructuration, with an editorial system and a more performing ergonomics of consultation.

A need, very soon, for new developments concerning new techniques in genetics.

Note: Some addresses

- New developments:http://atlasgeneticsoncology.org/News.html

- Atlas Journal Pdf/Scientific side of the Atlas:http://documents.irevues.inist.fr/handle/2042/15655

e.g. http://documents.irevues.inist.fr/bitstream/handle/2042/56473/vol_19_4_2015.pdf

- Cell Biology: e.g.http://atlasgeneticsoncology.org/Categories/DNA_repair.html

- Cell lines:http://atlasgeneticsoncology.org/cell_lines.html

- Nosology: http://atlasgeneticsoncology.org/Tumors/Solid_Nosology_9.html

- Physical maps of genes, markers, and diseases at the level of the chromosome band: e.g. http://atlasgeneticsoncology.org/Bands/21q22.html

[1]Given the magnitude of the task, it could be very tempting to limit the Atlas to only a part of it, let's say the leukemias part.

However, it would ruin a specificity/originality of the Atlas: bringing together the diverse and complementary knowledge, to offer a broader view concerning cancer genetics processes. All the more so as a gene can be translocated in a leukemia and overexpressed in a carcinoma, or the opposite, and as the t(16;21)(p11;q22) FUS/ERG may be found in the Ewing?PNET spectrum and in acute myeloid leukemia!.

Editorial workflow in the Atlas

2015-12-17T13:38:52+01:00

Editorial workflow in the Atlas

The Atlas editorial team stands in need of Section Editors (see http://atlasgeneticsoncology.org/BackpageAbout.html#EDITORIAL ) devoting 10% of their time for the Atlas.

The workflow detailed herein below applies when MSc students/workers are involved in the process. Indeed, a senior researcher will skim through the various steps described below. However a secretary's active watch on forthcoming papers from the various authors is needed (like an appointment calendar). Moreover, when the Atlas has evolved into a true database with an automated editorial process, many of these time consuming tasks will vanish.

I- Subject-by-subject expertise

For each of the themes included in the atlas (genes, leukemias, solid tumors, hereditary diseases involving increased risk of cancer, "deep insight" …), the editorial team is tasked with appraising the subjects (or "items") lending themselves to publication on the site.

As regards genes, for instance, using a predefined list of the genes potentially implicated in cancer (a list determined by algorithms for different data bases by Philippe Dessen, the data base manager), the editorial team is initially tasked with verifying the implication (or non-implication) of these genes in carcinogenesis. With this in mind, they study the existing bibliography, primarily on the basis of the information contained in PubMed. They then endeavor to determine whether or not the published data suffice to justify a detailed written review.

As regards the other themes (leukemias, solid tumors, hereditary diseases involving increased risk of cancer...), the bibliographic research is also carried out from PubMed, and also on specialized sites (Mitelman, Orphanet, OMIM, WHO, …). This research phase favors subjects for which enough recent publications are available to allow for high-quality reviews.

Finally, the editorial team decides whether or not a given subject will constitute an item justifying publication. After that, it is a matter of searching for and selecting the author in the best position to write this review.

II- Searching for the right author

Once a subject has been determined, the editorial team conducts a search of recent publications in view of choosing the author/the team in the best position to write something for the Atlas: their second appraisal. Concerning their choice, the following factors have got to be taken into account: number of publications by the author, the impact factor of his or her publications, and the author's status: clinician, hospital-based biologist, researcher. The author's disciplines are likewise taken into consideration: oncology, a specific organ, cytogenetic biology, molecular biology, cellular biology, physiopathology, etc. As regards teams, a multidisciplinary team will be preferred.

This is a highly sensitive step. According to the author chosen, the quality of the review is likely to vary, and its scientific orientation will be more or less fundamental or clinical.

Other selection criteria include: qualities of clarity in data presentation, synthesis and the use of schemas or medical imagery (in the broad sense of the word, including anatomopathology and chromosomes).

III- Managing the contact list spreadsheets - Managing the spreadsheet identifiers

Along with the different items (genes, leukemias, solid tumors...), all important data on the authors are conserved in dedicated files.

And for each gene, the spreadsheets inventory information on its implication, as well as all other information deemed useful for future research (authors to be contacted, their contact information, e-mail exchanges, agreement to write an article, speed in production, and subjects to be reserved for a given author...). Totally indispensable, the spreadsheets are of concrete use during each phase of the work. They need to be ergonomic, and evolve according to changing needs.

For each theme in the Atlas (Genes, Leukemias, Solid Tumors, Hereditary Diseases involving increased risk of cancer, "deep Insights", Teaching Chapters), there exists a dedicated spreadsheet.

Each spreadsheet provides a list of the subjects studied, the relevant dates, as well as the subjects to be studied, for which the right authors remain to be found.

The spreadsheets are updated daily, and new, potentially interesting subjects are added periodically. This supplementary material is enriched by readings of articles from the literature and by analysis of the articles received by the Atlas.

Each subject is designated by a specific and numbered identifier facilitating the establishment of internal links as the files are being edited.

Possible duplicate files are regularly sought out and subjected to analysis, and the spreadsheets are consequently "cleaned".

For an example, see below: Extracts from the "Genes" spreadsheet, which contains 9000 lines.

HOXA9 (7p15)	61	07p15	HOXA9	homeo box A9	t(7;11)/ANLL	done
PAX5 (9p13)	62	09p13	PAX5	paired box gene 5 (B-cell lineage specific activator protein)	t(9;14)/NHL	done
NUP98 (11p15)	63	11p15	NUP98	nucleoporin 98kDa	t(7;11)/ANLL	done
PICALM / CALM (11q21)	64	11q21	PICALM	phosphatidylinositol binding clathrin assembly protein	t(10;11)/ANLL	done
DDX6 / RCK / LPC (11q23)	65	11q23	DDX6	DEAD (Asp-Glu-Ala-Asp) box polypeptide 6	t(11;14)/NHL PMID 1394235	FOR SALE
TCL1A / TCL1 (14q32)	66	14q32	TCL1A	T-cell leukemia/lymphoma 1A	inv(14)ort(14;14)ort(X;14)/T-cell	done
BCL3 (19q13)	67	19q13	BCL3	B-cell CLL/lymphoma 3	t(14;19)/NHL/ChrLympho	Reserved
PAX7 (1p36.13)	68	01p36	PAX7	paired box gene 7	t(1;13)/rhabdo	FOR SALE
PRCC (1q21)	69	01q21	PRCC	papillary renal cell carcinoma (translocation-associated)	t(X;1)(p11;q21)renal carcinoma	done
PAX3 (2q35)	70	02q35	PAX3	paired box gene 3 (Waardenburg syndrome 1)	t(2;13)/rhabdo	done
CTNNB1 (3p21)	71	03p21	CTNNB1	catenin (cadherin-associated protein), beta 1, 88kDa	t(3;8)/adenoma PMID: 23490077, 24042511, 25124581	done
LPP (3q27)	72	03q27	LPP	LIM domain containing preferred translocation partner in lipoma	t(3;12)/lipoma	done
ETV1 (7p22)	73	07p22	ETV1	ets variant gene 1	t(7;22)/Ewing	done
PLAG1 (8q12)	74	08q12	PLAG1	pleiomorphic adenoma gene 1	t(3;8)/adenoma	done
NR4A3 / TEC / CHN (9q22)	75	09q22	NR4A3	nuclear receptor subfamily 4, group A, member 3	Extraskeletal myxoid chondrosarcoma with t(9;22)(q22;q12) or t(9;17)(q22;q11) or t(9;15)(q22;q21)	done
RET (10q11)	76	10q11	RET	ret proto-oncogene (multiple endocrine neoplasia and medullary thyroid carcinoma 1, Hirschsprung disease)	inv(10)/adenocar thyroid	done
AKAP10 / RIa (17q23-24)	77	17q23	AKAP10	A kinase (PRKA) anchor protein 10	thyroid	FOR SALE
WT1 (11p13)	78	11p13	WT1	Wilms tumor 1	t(11;22)/desmoplastic	done
FLI1 (11q24)	79	11q24	FLI1	Friend leukemia virus integration 1	t(11;22)/Ewing/PNET	done
DDIT3 / CHOP (12q13)	80	12q13	DDIT3	DNA-damage-inducible transcript 3	t(12;16)/liposarc	done
ATF1(12q13)	81	12q13	ATF1	activating transcription factor 1	t(12;22)/clear cell sarc	done

IV- Contacting the author - Managing author responses -

The authors are contacted through a common e-mail account using predetermined contact e-mail coordinates.

The e-mails are sent once a week, at the beginning of the week, as it has been observed that the highest response rate occurs at that time. On the same token, some times of the year are not conducive to soliciting authors who tend to be busy with applications for grants ... or on holiday. These periods are avoided as much as possible.

When an author fails to answer, he is re-contacted two or three times. If, after that, he still fails to answer, another author is sought out...

Author response statistics: 55% of the authors do not respond to the invitation; 25% of them refuse; 20% agree.

When authors refuse or do not respond, the process of searching for the right author is reinitiated. If no other author can or will write the requested review, the team will wait for new research to be published..

When, on the other hand, an author accepts, the team consults him on the time frame he thinks he shall need prior to sending his completed article. The publishing flow is thereby managed, both for the Internet site and the PDF journal. A model of writing for the review is given the author, who concomitantly receives relevant editorial information.

Quite frequently, articles fail to arrive within the allotted time. The status of ongoing articles has got to be regularly monitored, and reminder notes need to be sent.

It also often happens that notwithstanding an initially positive response, authors do not respond to reminder notes, or else they withdraw from the project. In those cases, search for the right author resumes.

Assistance for authors: Quite frequently, authors ask questions (deadlines , explanations pertaining to various details...) that call for timely responses.

V- Receipt of the worksheets - Flow management

Once the article has been received, the completed worksheet is registered on a common server.

The information is also recorded on common spreadsheets, in a common notebook dedicated to the editors' ongoing activities; it is also displayed on wall calendars providing overall perspective on publication flows.

With these calendars, the editorial team can rapidly apprise itself of a possible lack of articles for the PDF journals and try to optimally manage the flow of arriving articles. Unfortunately, given the fact that the authors are the ones who determine their sending dates, substantial variations in publication flow may come to exist, and not be easy to manage.

VI- Verification of the articles and assessment by referees (referring process)

The articles received are reread by internal referees; 97% of them (in fact all the articles, except for clinical case reports) are reviews of the literature written at the request of the Atlas editorial board; they are known as "commissioned papers". It should be noted that the authors were preselected according to rigorously applied criteria preliminarily to their writing of an article. Following receipt, the process of rereading and assessment of articles is implemented by the Atlas editorial board. It should also be noted that as the process draws to a close, the board member having chosen the subject (and subsequently the author himself) possesses a precise overall vision as to what the article is supposed to produce (quantity of knowledge in molecular biology or clinical research on a given gene...).

Articles that do not correspond to the publication criteria or that do not provide a sufficiently detailed report on the knowledge available on the subject are sent back for revision. The editorial team remains vigilant, and about 20% of the articles submitted are indeed sent back for revision. It is often necessary to send reminders to the authors, before receiving the revised version (loss of time).

The clinical case studies in hematology (the remaining 3%) are subjected to an external assessment process involving 4 or 5 experts, while the final decision is made by the Atlas editor-in-chief. Practically all the clinical case studies are reviewed by the authors at least one time prior to publication; only 8% are immediately accepted, 68% are accepted following revision, and 24% of the articles having been submitted are finally refused.

VII- Publication of the articles - html coding

Once the articles have been accepted, they are processed so that they can be placed on line by the data base manager.

The articles are to be formatted according to a strictly applied computational model in order to be properly handled by the scripts of the data base manager (see, as an example, the form below).

The text must be painstakingly reread so as to correct possible mistakes (typos, grammar, spelling...), and each bibliographical reference cited in the next has got to be verified and corrected (if need be).

The article header (the different tags or tracking devices allowing for indexing of the form in different parts of the data base in accordance with different criteria) must be carefully filled out, using the metadata contained in the article. The metadata will permit the data base manager to integrate the form within the site so that it can be inventoried with regard to the dedicated lists.

The articles in the Atlas must follow a predetermined model; each paragraph of the review must be included within the tags, and the text must be formatted according to a computer encoding system. Special characters (accent marks, Greek letters, symbols…ex: integrin ανβ3) must be coded in the HTML format so that their posting on the website be correct.

In the text itself, all potential internal links to other items contained in the Atlas (genes, leukemias, solid tumors...) must be identified, and internal links created in such a way that readers are directed, if they wish, to other articles in the Atlas. New subjects for the Atlas are often found while the forms are being processed, and added to the shared spreadsheets.

Most often, the bibliography contains 50 to 100 references, and it has got to be processed in a predetermined format.

The articles also contain images, which are processed by Photoshop software. More often than not, the size of the images requires rectification, and the background of the image has got to be rendered transparent. Moreover, the text may need rewriting when it is too blurry or has been degraded due to the change in size.

Once processing of the worksheet has been completed, it is put through a simulator so as to verify the correctness of its formatting, and also so as to make sure that no component remains invisible, as happens when a closing tag such as > is forgotten.

The file and the attached images are then sent for validation to Jean-Loup Huret, the editor-in-chief, and subsequently to the data base manager for uploading or posting on line.

"Deep Insight" and "Educational items" constitute special cases. As these files are "free format" and do not correspond to a precise model, they are directly processed using specialized software (the Dreamweaver website-editing software) in the HTML format. For these files, it is necessary to carry out all coding and page layout in HTML.

Example below : Partial formatting of an article: In the example given below, any and all parts of the text in color are subjected to special processing.

BEGIN_HEADER

FILENAMESH3PXD2AID45995ch10q24.txt

CLASSE GENE

ID45995

LOCUSID

TRI_PAR_CHROMOSOME10

TRANSLOC t(10;10)(q24;q24) SH3PXD2A/OBFC1

TRANSLOC t(10;13)(q24;q14) SH3PXD2A/RB1

FUSION_GENESH3PXD2A/OBFC1

FUSION_GENESH3PXD2A/RB1

CATEGORYCytoskeleton

END_HEADER

etc..

etc...

FUNCTIONTKS5 was initially identified as a substrate for <CC: TXT:SRC ID: 448> (Lock et al., 1998), and was subsequently shown to play a critical role in invadosome formation in multiple cell types (Courtneidge, 2011; Murphy and Courtneidge, 2011; Paz et al., 2013). <BR>

FUNCTIONFull-length TKS5 functions as an adaptor for recruiting other proteins to the cell membrane for invadosome formation. The recruitment of TKS5 to the cell membrane depends on its PX domain and phosphorylation by Src (Abram et al., 2003). It has been proposed that phosphorylation of TKS5 releases its PX domain from intramolecular interaction and allows TKS5 to bind to cell membrane phosphatidylinositol lipids, such as phosphatidylinositol-3,4-bisphosphate (PI(3,4)P₂) (Abram et al., 2003; Oikawa et al., 2008). At the cell membrane, TKS5 is thought to interact with multiple components of invadosomes either directly or indirectly, and thereby mediates invadosome formation and maturation (Sharma et al., 2013). These interacting partners includes adaptor proteins and actin regulatory proteins, such as <CC: TXT:NCK1 ID:41505>, <CC: TXT:NCK2 ID:52582>, <CC: TXT:GRB2 ID: 386>, <CC: TXT: CTTN ID: 369> (Cortactin), <CC: TXT: WASL ID: 42803> (N-WASP), <CC: TXT: ACTR2ID: 49744<CC: TXT: ACTR3ID:46303> (Arp2/3) complex, and <CC: TXT: ARHGAP35 ID: 52237> (p190RhoGAP) (Crimaldi et al., 2009; Oikawa et al., 2008; Stylli et al., 2009).<BR>

FUNCTION TKS5 also interacts with <CC: TXT:NOXA1 ID:41563> and <CC: TXT: CYBA ID: 43882> (p22phox), which are components of the NADPH oxidase complex, and thereby promotes reactive oxygen species (ROS) production by NOX enzymes at invadosomes (Diaz et al., 2009; Gianni et al., 2010; 2009).ROS have been shown to facilitate invadosome formation by maintaining or amplifying the phosphorylation of TKS5. As such, TKS5 is thought to promote invadosome formation via ROS in a positive feedback loop.<BR>

FUNCTION Finally, TKS5 has also been shown to interact with members of the ADAM family metalloproteases, specifically <CC: TXT:ADAM12 ID:44084>, <CC: TXT:ADAM15 ID:46345>, <CC: TXT:ADAM19 ID:46837>(Abram et al., 2003). It is believed that Tks5 recruits theses proteases to the invadosome foci for processing growth factors and regulating cell motility. For example, ADAM12 has been shown to promote ectodomain shedding of <CC: TXT:HBEGF ID: 40369> (heparin-binding EGF-like growth factor) and enhance invadopodia formation in cancer cells (Diaz et al., 2013). <BR>

etc...

VIII- Posting (uploading) and verification

Article upload takes place virtually every week, and for each article, it has to be verified. Also to be verified: Has the article been correctly indexed in the dedicated lists? Has the article been correctly displayed? .

IX- Author acknowledgment

Before a thank-you e-mail is sent to the authors of a review, their bibliographies are searched so as to see if they could possibly be tasked with another review. If this is the case, they are asked whether or not they would be interested in pursuing their collaboration.

The author is given the address at which he can find his review on the Atlas site.

X- Creation and management of the PDF journal

http://documents.irevues.inist.fr/handle/2042/15655

Prior to each issue, the editor in charge of the journal is tasked with creating the table of contents and scrupulously selecting the articles to be published. This is because publishing workflow is highly fluctuating, and consequently demands "hands-on" management.

A tool for the future data base carrying out initial formatting of the articles and editing the table of contents provides assistance in the page layout of the PDF journal.

In each issue, page layout is a sensitive matter. It is performed article by article, and has got to be done in such a way that a given issue is harmonious and satisfactorily balanced; moreover, image management must ensure maximal quality.

Once the journal is formatted and paginated, it is validated by the editor-in-chief.

The issue is then sent to the INIST-CNRS for finalizing of the PDF. The INIST editors recover the meta-data for the articles and associate them with the issue. They are also tasked with assigning the DOI (digital object identifier) for each article that will serve as its single identification number.

For back-up purposes, this final PDF is registered on the future data base.

Once all of the above steps have been carried out, the authors are contacted anew and informed of the publication of their articles in the journal and the link to the latter in PDF with which they are being provided.

Table of working time distribution for each Atlas editor (in percentage, for full-time service: 35h/week

Task	% Equivalent full time
Subject expertise	94
Search for authors	30
Contact list spreadsheet management	42
Contacting authors	47
Managing author responses	39
Managing the spreadsheet identifiers	16
Receipt of the worksheet forms	5
Verification and assessment of the articles	tio
Publication of the articles	125
Uploading and verification of the articles	15
Addressing acknowledgements to the authors	15
Integration of the new site (BDD)	10
Creation and management of a PDF journal	10
Management and development of the new site (BDD)	10
Management of association members and donations	5
Management and maintenance of the promotional site	1
Maintenance and development of the current site	9
Miscellaneous	10
TOTAL	500

The above percentages are subject to modification according to editorial needs and the fluctuating importance of certain tasks.

Again, we want to make it clear that the workflow detailed herein applies when MSc students/workers are involved in the process. Indeed, a senior researcher will skim through the various steps. However a secretary's active watch on forcoming papers is needed. Moreover, when the Atlas has evolved into a true database with an automated editorial process, many of these time consuming tasks will vanish.

The Atlas can run with:

- an Editor in Chief (20% full-time) + secretary (2-5%).

- Section Editors (5- 10% full-time) + secretary (1%).

- a Bio-computer specialist (10% full time).

- .. and as many good authors as possible !

Atlas Support 2015

2015-12-10T16:07:30+01:00

To all Cytogeneticists, Geneticists, Clinicians, and Scientists for whom the Atlas of Genetics and Cytogenetics in Oncology and Hematology still represents a cultural and practical tool ...

see: http://atlasgeneticsoncology.org//Supporting_Atlas_First_signatories.pdf

Chromosomes in Cancer - How to contact us

Submission Form to Bibliographic Databases

JOURNAL SUBMISSION FORM

Title: Atlas of Genetics and Cytogenetics in Oncology and Haematology URL: http://AtlasGeneticsOncology.org

I- Editor and Publisher

II- Publishing Standards

III- Editorial policies

IV- Quality of its contents and editorial processes

Templates_for_cards-papers

TEMPLATES

TEMPLATE for GENES

II- TEMPLATE for LEUKEMIAS

III- TEMPLATE for SOLID TUMORS

IV- TEMPLATE for CANCER-PRONE DISEASES

Atlas Submission to Bibliographic Databases

JOURNAL SUBMISSION FORM

Title: Atlas of Genetics and Cytogenetics in Oncology and Haematology

Journal: http://irevues.inist.fr/atlasgeneticsoncology

I- Editor and Publisher

II- Publishing Standards

III- Editorial policies

IV- Quality of its contents and editorial processes

MainScriptsofAtlas

Atlas website structure

Atlas Users

Argument

Atlas Added Value

Editorial workflow in the Atlas

The Atlas can run with:

- an Editor in Chief (20% full-time) + secretary (2-5%).

- Section Editors (5- 10% full-time) + secretary (1%).

- a Bio-computer specialist (10% full time).

- .. and as many good authors as possible !

Atlas Support 2015

Title: Atlas of Genetics and Cytogenetics in Oncology and Haematology
URL: http://AtlasGeneticsOncology.org