Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)-Reference-Cited by-同舟云学术

Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

Published:2022-05 Issue:5 Volume:24 Page:986-998
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Horak Peter,Griffith Malachi,Danos Arpad M.,Pitel Beth A.,Madhavan Subha,Liu Xuelu,Chow Cynthia,Williams Heather,Carmody Leigh,Barrow-Laing Lisa,Rieke Damian,Kreutzfeldt Simon,Stenzinger Albrecht,Tamborero David,Benary Manuela,Rajagopal Padma Sheila,Ida Cristiane M.,Lesmana Harry,Satgunaseelan Laveniya,Merker Jason D.,Tolstorukov Michael Y.,Campregher Paulo Vidal,Warner Jeremy L.,Rao Shruti,Natesan Maya,Shen Haolin,Venstrom Jeffrey,Roy Somak,Tao Kayoko,Kanagal-Shamanna Rashmi,Xu Xinjie,Ritter Deborah I.,Pagel Kym,Krysiak Kilannin,Dubuc Adrian,Akkari Yassmine M.,Li Xuan Shirley,Lee Jennifer,King Ian,Raca Gordana,Wagner Alex H.,Li Marylin M.,Plon Sharon E.,Kulkarni Shashikant,Griffith Obi L.,Chakravarty Debyani,Sonkin Dmitriy^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference41 articles.

1. Standards and guidelines for the interpretation and reporting of sequence variants in cancer: a joint consensus recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists;Li;J Mol Diagn,2017

2. A framework to rank genomic alterations as targets for cancer precision medicine: the ESMO Scale for Clinical Actionability of molecular Targets (ESCAT);Mateo;Ann Oncol,2018

3. CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer;Griffith;Nat Genet,2017

4. OncoKB: a precision oncology knowledge base;Chakravarty;JCO Precis Oncol,2017

5. A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer;Wagner;Nat Genet,2020

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