Correspondence on "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)" by Horak et al Response

被引：0

作者：

Horak, Peter ^{[1
]}

Chakravarty, Debyani ^{[2
]}

Sonkin, Dmitriy ^{[3
]}

机构：

[1] Natl Ctr Tumor Dis NCT, Neuenheimer Feld 460, D-69120 Heidelberg, Germany

[2] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10065 USA

[3] NCI, Rockville, MD 20850 USA

来源：

GENETICS IN MEDICINE | 2022年 / 24卷 / 09期

关键词：

D O I：

10.1016/j.gim.2022.05.018

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1989 / 1990

页数：2

共 4 条

[1] 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) [J].

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 .

GENETICS IN MEDICINE, 2022, 24 (05) :986-998

[2] A standard operating procedure for the interpretation of oncogenicity/pathogenicity of somatic mutations [J].

Horak, Peter ;

Griffith, Malachi ;

Danos, Arpad ;

Pitel, Beth A. ;

Madhavan, Subha ;

Liu, Xuelu ;

Lee, Jennifer ;

Raca, Gordana ;

Li, Shirley ;

Wagner, Alex H. ;

Kulkarni, Shashikant ;

Griffith, Obi L. ;

Chakravarty, Debyani ;

Sonkin, Dmitriy .

CANCER RESEARCH, 2020, 80 (16)

[3]

Mehta N, 2022, GENET MED, DOI [10.1016/j.gim.2022.05, DOI 10.1016/J.GIM.2022.05]

[4] Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology [J].

Richards, Sue ;

Aziz, Nazneen ;

Bale, Sherri ;

Bick, David ;

Das, Soma ;

Gastier-Foster, Julie ;

Grody, Wayne W. ;

Hegde, Madhuri ;

Lyon, Elaine ;

Spector, Elaine ;

Voelkerding, Karl ;

Rehm, Heidi L. .

GENETICS IN MEDICINE, 2015, 17 (05) :405-424

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