Literature DB >> 32720330

Fitting a naturally scaled point system to the ACMG/AMP variant classification guidelines.

Sean V Tavtigian1,2, Steven M Harrison3, Kenneth M Boucher2,4, Leslie G Biesecker5.   

Abstract

Recently, we demonstrated that the qualitative American College of Medical Genetics and Genomics/Association for Medical Pathology (ACMG/AMP) guidelines for evaluation of Mendelian disease gene variants are fundamentally compatible with a quantitative Bayesian formulation. Here, we show that the underlying ACMG/AMP "strength of evidence categories" can be abstracted into a point system. These points are proportional to Log(odds), are additive, and produce a system that recapitulates the Bayesian formulation of the ACMG/AMP guidelines. The strengths of this system are its simplicity and that the connection between point values and odds of pathogenicity allows empirical calibration of the strength of evidence for individual data types. Weaknesses include that a narrow range of prior probabilities is locked in and that the Bayesian nature of the system is inapparent. We conclude that a points-based system has the practical attribute of user-friendliness and can be useful so long as the underlying Bayesian principles are acknowledged.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  ACMG; Bayesian framework; VUS; medical genetics; points-based classification system; scoring metric; unclassified variants; variant classification; variants of uncertain significance

Mesh:

Substances:

Year:  2020        PMID: 32720330      PMCID: PMC8011844          DOI: 10.1002/humu.24088

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.700


  8 in total

1.  Analysis of missense variation in human BRCA1 in the context of interspecific sequence variation.

Authors:  V Abkevich; A Zharkikh; A M Deffenbaugh; D Frank; Y Chen; D Shattuck; M H Skolnick; A Gutin; S V Tavtigian
Journal:  J Med Genet       Date:  2004-07       Impact factor: 6.318

2.  Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2.

Authors:  David E Goldgar; Douglas F Easton; Amie M Deffenbaugh; Alvaro N A Monteiro; Sean V Tavtigian; Fergus J Couch
Journal:  Am J Hum Genet       Date:  2004-08-02       Impact factor: 11.025

3.  A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.

Authors:  Douglas F Easton; Amie M Deffenbaugh; Dmitry Pruss; Cynthia Frye; Richard J Wenstrup; Kristina Allen-Brady; Sean V Tavtigian; Alvaro N A Monteiro; Edwin S Iversen; Fergus J Couch; David E Goldgar
Journal:  Am J Hum Genet       Date:  2007-09-06       Impact factor: 11.025

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.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

5.  Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Authors:  Keith Nykamp; Michael Anderson; Martin Powers; John Garcia; Blanca Herrera; Yuan-Yuan Ho; Yuya Kobayashi; Nila Patil; Janita Thusberg; Marjorie Westbrook; Scott Topper
Journal:  Genet Med       Date:  2017-05-11       Impact factor: 8.822

6.  Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).

Authors:  Erin Rooney Riggs; Erica F Andersen; Athena M Cherry; Sibel Kantarci; Hutton Kearney; Ankita Patel; Gordana Raca; Deborah I Ritter; Sarah T South; Erik C Thorland; Daniel Pineda-Alvarez; Swaroop Aradhya; Christa Lese Martin
Journal:  Genet Med       Date:  2019-11-06       Impact factor: 8.822

7.  Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework.

Authors:  Sean V Tavtigian; Marc S Greenblatt; Steven M Harrison; Robert L Nussbaum; Snehit A Prabhu; Kenneth M Boucher; Leslie G Biesecker
Journal:  Genet Med       Date:  2018-01-04       Impact factor: 8.822

8.  Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.

Authors:  Sharon E Plon; Diana M Eccles; Douglas Easton; William D Foulkes; Maurizio Genuardi; Marc S Greenblatt; Frans B L Hogervorst; Nicoline Hoogerbrugge; Amanda B Spurdle; Sean V Tavtigian
Journal:  Hum Mutat       Date:  2008-11       Impact factor: 4.878

  8 in total
  14 in total

1.  A calibrated functional patch-clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome.

Authors:  Connie Jiang; Ebony Richardson; Jessica Farr; Adam P Hill; Rizwan Ullah; Brett M Kroncke; Steven M Harrison; Kate L Thomson; Jodie Ingles; Jamie I Vandenberg; Chai-Ann Ng
Journal:  Am J Hum Genet       Date:  2022-06-09       Impact factor: 11.043

2.  Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutions.

Authors:  Kathleen A Clark; Andrew Paquette; Kayoko Tao; Russell Bell; Julie L Boyle; Judith Rosenthal; Angela K Snow; Alex W Stark; Bryony A Thompson; Joshua Unger; Jason Gertz; Katherine E Varley; Kenneth M Boucher; David E Goldgar; William D Foulkes; Alun Thomas; Sean V Tavtigian
Journal:  Am J Hum Genet       Date:  2022-06-02       Impact factor: 11.043

3.  Minigene Splicing Assays Identify 20 Spliceogenic Variants of the Breast/Ovarian Cancer Susceptibility Gene RAD51C.

Authors:  Lara Sanoguera-Miralles; Elena Bueno-Martínez; Alberto Valenzuela-Palomo; Ada Esteban-Sánchez; Inés Llinares-Burguet; Pedro Pérez-Segura; Alicia García-Álvarez; Miguel de la Hoya; Eladio A Velasco-Sampedro
Journal:  Cancers (Basel)       Date:  2022-06-15       Impact factor: 6.575

4.  The p.Ser64Leu and p.Pro104Leu missense variants of PALB2 identified in familial pancreatic cancer patients compromise the DNA damage response.

Authors:  Yue Zhang; Jung-Young Park; Fan Zhang; Sara H Olson; Irene Orlow; Yirong Li; Robert C Kurtz; Marc Ladanyi; Jie Chen; Amanda E Toland; Liying Zhang; Paul R Andreassen
Journal:  Hum Mutat       Date:  2020-12-16       Impact factor: 4.878

Review 5.  Monogenic diabetes: a gateway to precision medicine in diabetes.

Authors:  Haichen Zhang; Kevin Colclough; Anna L Gloyn; Toni I Pollin
Journal:  J Clin Invest       Date:  2021-02-01       Impact factor: 14.808

6.  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).

Authors:  Peter Horak; Malachi Griffith; Arpad M Danos; Beth A Pitel; Subha Madhavan; Xuelu Liu; Cynthia Chow; Heather Williams; Leigh Carmody; Lisa Barrow-Laing; Damian Rieke; Simon Kreutzfeldt; Albrecht Stenzinger; David Tamborero; Manuela Benary; Padma Sheila Rajagopal; Cristiane M Ida; Harry Lesmana; Laveniya Satgunaseelan; Jason D Merker; Michael Y Tolstorukov; Paulo Vidal Campregher; Jeremy L Warner; Shruti Rao; Maya Natesan; Haolin Shen; Jeffrey Venstrom; Somak Roy; Kayoko Tao; Rashmi Kanagal-Shamanna; Xinjie Xu; Deborah I Ritter; Kym Pagel; Kilannin Krysiak; Adrian Dubuc; Yassmine M Akkari; Xuan Shirley Li; Jennifer Lee; Ian King; Gordana Raca; Alex H Wagner; Marylin M Li; Sharon E Plon; Shashikant Kulkarni; Obi L Griffith; Debyani Chakravarty; Dmitriy Sonkin
Journal:  Genet Med       Date:  2022-01-29       Impact factor: 8.864

7.  Evaluating the impact of in silico predictors on clinical variant classification.

Authors:  Emma H Wilcox; Mahdi Sarmady; Bryan Wulf; Matt W Wright; Heidi L Rehm; Leslie G Biesecker; Ahmad N Abou Tayoun
Journal:  Genet Med       Date:  2021-12-23       Impact factor: 8.864

8.  Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.

Authors:  Lucy Loong; Cankut Cubuk; Subin Choi; Sophie Allen; Beth Torr; Alice Garrett; Chey Loveday; Miranda Durkie; Alison Callaway; George J Burghel; James Drummond; Rachel Robinson; Ian R Berry; Andrew Wallace; Diana M Eccles; Marc Tischkowitz; Sian Ellard; James S Ware; Helen Hanson; Clare Turnbull
Journal:  Genet Med       Date:  2021-11-18       Impact factor: 8.864

9.  Computational and experimental methods for classifying variants of unknown clinical significance.

Authors:  Malte Spielmann; Martin Kircher
Journal:  Cold Spring Harb Mol Case Stud       Date:  2022-04-28

10.  Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations.

Authors:  Alice Garrett; Miranda Durkie; Alison Callaway; George J Burghel; Rachel Robinson; James Drummond; Bethany Torr; Cankut Cubuk; Ian R Berry; Andrew J Wallace; Sian Ellard; Diana M Eccles; Marc Tischkowitz; Helen Hanson; Clare Turnbull
Journal:  J Med Genet       Date:  2020-11-18       Impact factor: 5.941

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