Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants

被引:191
作者
Jarvik, Gail P. [1 ,2 ]
Browning, Brian L. [1 ,2 ]
机构
[1] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[2] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
关键词
SEQUENCE VARIANTS;
D O I
10.1016/j.ajhg.2016.04.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The American College of Medical Genetics and Genomics (ACMG) and Association of Molecular Pathology (AMP) recently published important new guidelines aiming to improve and standardize the pathogenicity classification of genomic variants. The Clinical Sequencing Exploratory Research (CSER) consortium evaluated the use of these guidelines across nine laboratories. One identified obstacle to consistent usage of the ACMG-AMP guidelines is the lack of a definition of cosegregation as criteria for pathogenicity classification. Cosegregation data differ from many other types of pathogenicity data in being quantitative. However, the ACMG-AMP guidelines do not define quantitative criteria for use of these data. Here, such quantitative criteria, in an easily implementable form, are proposed.
引用
收藏
页码:1077 / 1081
页数:5
相关论文
共 50 条
  • [41] Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling-a Singaporean experience
    Chin, Hui-Lin
    Lam, Joyce Ching Mei
    Christopher, Dheepa
    Michelle, Poon Limei
    Junrong, Benedict Yan
    FRONTIERS IN ONCOLOGY, 2023, 13
  • [42] iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers
    Wang, Meng
    Wei, Liping
    SCIENTIFIC REPORTS, 2016, 6
  • [43] SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population
    Moreno-Cabrera, Jose M.
    Feliubadalo, Lidia
    Pineda, Marta
    Prada-Dacasa, Patricia
    Ramos-Muntada, Mireia
    Del Valle, Jesus
    Brunet, Joan
    Gel, Bernat
    Curras-Freixes, Maria
    Calsina, Bruna
    Salazar-Hidalgo, Milton E.
    Rodriguez-Balada, Marta
    Roig, Barbara
    Fernandez-Castillejo, Sara
    Duran Dominguez, Mercedes
    Arranz Ledo, Monica
    Infante Sanz, Mar
    Castillejo, Adela
    Damaso, Estela
    Soto, Jose L.
    de Miguel, Montserrat
    Hidalgo Calero, Beatriz
    Sanchez-Zapardiel, Jose M.
    Ramon Y Ramon, Teresa
    Lasa, Adriana
    Gisbert-Beamud, Alexandra
    Lopez-Novo, Anael
    Ruiz-Ponte, Clara
    Potrony, Miriam
    Alvarez-Mora, Maria, I
    Osorio, Ana
    Lorda-Sanchez, Isabel
    Robledo, Mercedes
    Cascon, Alberto
    Ruiz, Anna
    Spataro, Nino
    Hernan, Imma
    Borras, Emma
    Moles-Fernandez, Alejandro
    Earl, Julie
    Cadinanos, Juan
    Sanchez-Heras, Ana B.
    Bigas, Anna
    Capella, Gabriel
    Lazaro, Conxi
    DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION, 2024, 2024
  • [44] Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance
    Richardson, Marcy E.
    Hu, Chunling
    Lee, Kun Y.
    LaDuca, Holly
    Fulk, Kelly
    Durda, Kate M.
    Deckman, Ashley M.
    Goldgar, David E.
    Monteiro, Alvaro N. A.
    Gnanaolivu, Rohan
    Hart, Steven N.
    Polley, Eric C.
    Chao, Elizabeth
    Pesaran, Tina
    Couch, Fergus J.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2021, 108 (03) : 458 - 468
  • [45] Genetic Prostate Cancer Risk Assessment: Common Variants in 9 Genomic Regions are Associated With Cumulative Risk
    Helfand, Brian T.
    Fought, Angela J.
    Loeb, Stacy
    Meeks, Joshua J.
    Kan, Donghui
    Catalona, William J.
    JOURNAL OF UROLOGY, 2010, 184 (02) : 501 - 505
  • [46] Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants
    Brasil, Sandra
    Leal, Fatima
    Vega, Ana
    Navarrete, Rosa
    Jesus Ecay, Maria
    Desviat, Lourdes R.
    Riera, Casandra
    Padilla, Natalia
    de la Cruz, Xavier
    Luz Couce, Mari
    Martin-Hernandez, Elena
    Morais, Ana
    Pedron, Consuelo
    Pena-Quintana, Luis
    Rigoldi, Miriam
    Specola, Norma
    Tavares de Almeida, Isabel
    Vives, Inmaculada
    Yahyaoui, Raquel
    Rodriguez-Pombo, Pilar
    Ugarte, Magdalena
    Perez-Cerda, Celia
    Merinero, Begona
    Perez, Belen
    ORPHANET JOURNAL OF RARE DISEASES, 2018, 13
  • [47] Functional characterization of 105 factor H variants associated with aHUS: lessons for variant classification
    Martin Merinero, Hector
    Zhang, Yuzhou
    Arjona, Emilia
    Del Angel, Guillermo
    Goodfellow, Renee
    Gomez-Rubio, Elena
    Ji, Rui-Ru
    Michelena, Malkoa
    Smith, Richard J. H.
    Rodriguez de Cordoba, Santiago
    BLOOD, 2021, 138 (22) : 2185 - 2201
  • [48] Saturation genome editing-based clinical classification of BRCA2 variants
    Sahu, Sounak
    Galloux, Melissa
    Southon, Eileen
    Caylor, Dylan
    Sullivan, Teresa
    Arnaudi, Matteo
    Zanti, Maria
    Geh, Josephine
    Chari, Raj
    Michailidou, Kyriaki
    Papaleo, Elena
    Sharan, Shyam K.
    NATURE, 2025, : 538 - 545
  • [49] Accessing clinical-grade genomic classification data through the ClinGen Data Platform
    Dalton, Karen P.
    Rehm, Heidi L.
    Wright, Matt W.
    Mandell, Mark E.
    Krysiak, Kilannin
    Babb, Lawrence
    Riehle, Kevin
    Nelson, Tristan
    Wagner, Alex H.
    BIOCOMPUTING 2023, PSB 2023, 2023, : 531 - 535
  • [50] Classification and Clinical Management of Variants of Uncertain Significance in High Penetrance Cancer Predisposition Genes
    Moghadasi, Setareh
    Eccles, Diana M.
    Devilee, Peter
    Vreeswijk, Maaike P. G.
    van Asperen, Christi J.
    HUMAN MUTATION, 2016, 37 (04) : 331 - 336