The Compendium of Cancer Genome Aberrations: Difference between revisions
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'''Welcome to the CCGA!''' | |||
<br /> | *An open resource focused on describing clinically relevant chromosomal and genomic abnormalities in cancer | ||
*Intended as a companion resource to the [https://tumourclassification.iarc.who.int/welcome/ WHO Classification of Tumours (WCT)] book series | |||
*Provides clinically significant genetic information for entities based on the current WCT disease ontology | |||
*Supported by the [https://www.cancergenomics.org/ Cancer Genomics Consortium (CGC)] and in collaboration with [https://whobluebooks.iarc.fr/about/ IARC] (publisher of the WCT book series) | |||
*Crowdsourced using a wiki-style interface, allowing for real-time editing and content sharing | |||
*Contributed to by colleagues with an interest in clinical cytogenetics, molecular genetics and genomics in cancer ([https://mms.cancergenomics.org/members/form.php?orgcode=CGC&fid=3830649 Volunteer Form]) | |||
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{{Box-round|titleforeground=white|titlebackground=#003399|title=Search Content Structured Based on the WHO Classification of Tumours (click book images below)|view-link=MediaWiki|content= Reference: [WHO Classification of Tumours.|Reference: [https://tumourclassification.iarc.who.int/welcome/ WHO Classification of Tumours.] The hierarchical tumour classification structure is reproduced with permission from the copyright holder, [https://whobluebooks.iarc.fr/about/ ©International Agency for Research on Cancer.]}}<div style=" | |||
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"><div style="flex: 0 1 calc(20% - 10px);">[[File:Haem.png|frameless|class=responsive-img|link=HAEM5:Table of Contents]]</div> | |||
<div style="flex: 0 1 calc(20% - 10px);">[[File:CNS.png|frameless|class=responsive-img|link=CNS5:Table of Contents]]</div> | |||
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[[File:CGC logo only.png|100px|link=Main_Page]]<span id="fp-span-cgc-pre"> '''CGC Workgroups Recurrent Loci Tables'''</span><span id="fp-span-cgc" style="display: block; margin-top: -62px; margin-left: 385px;"> [[AML Table: Recurrent Genomic Alterations Detected by Chromosomal Microarray|AML]] | [[MDS, MDS/MPN and MPN Tables: Recurrent Genomic Alterations Detected by Chromosomal Microarray|MDS/MPN]] | [[CLL Tables: Regions of Recurrent Copy Number Change and CN-LOH|CLL]] | [[Recurrent Genomic Alterations in Pediatric and Adult Central Nervous System Tumors Detected by Chromosomal Microarray|CNS Tumors]] | [[Plasma Cell Neoplasms Tables: Recurrent Cytogenomic Alterations|Plasma Cell Neoplasms]] | [[Breast Cancer: Recurrent Genomic Alterations|Breast Cancer]] | [[Renal Cell Neoplasia Tables: Recurrent Cytogenomic Alterations|Renal Neoplasia]] | [[B-ALL Tables: Prognostic Genomic Abnormalities and Recurrent Gene Fusions|B-ALL]]</span> | |||
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<h4>Author Resources</h4> | |||
- [[Author Instructions]] | |||
- [[Video Tutorials]] | |||
- [[Volunteer_Assignments_and_Opportunities|Authorship Assignment]] | |||
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<h4>Join Us!</h4> | |||
- [[About Us]] | |||
- [https://mms.cancergenomics.org/members/form.php?orgcode=CGC&fid=3830649 Volunteer Form] | |||
- [[Description_of_CCGA_Roles|Role Descriptions]] | |||
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<h4>Frequently Asked Questions</h4> | |||
- [[Frequently Asked Questions (FAQs)|FAQs]] | |||
- [[Contact us|Contact Us]] | |||
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