Literature DB >> 26239817

The genomic birthday paradox: how much is enough?

Peter Krawitz1,2, Orion Buske3,4, Na Zhu1, Michael Brudno3,4, Peter N Robinson1,2,5,6.   

Abstract

Genomic matchmaking databases (GMDs) allow participants to submit genomic and phenotypic data with the goal of identifying previously uncharacterized disease-associated genes by "matching" to other comparable cases. Current estimates suggest that there are at least 3,000 Mendelian disease-associated genes that have not yet been characterized as such, but the true number may be substantially higher. Therefore, GMDs are addressing a pressing medical need, and it is important to ask how they should be designed and how much data they should strive to contain in order to identify a certain number of these genes. In this work, we argue that genomic matchmaking has similarities to the so-called "birthday paradox," which refers to the observation that within a group of just 23 persons, two people will have the same birthday with probability greater than 50%. We develop a series of simulations to provide a rough estimate of the number of cases required and to explore the influence of parameters such as genetic heterogeneity, mode of inheritance, background variation, precision of phenotypic descriptions, disease prevalence, and the accuracy of bioinformatics pathogenicity prediction programs on the performance of genomic matchmaking.
© 2015 WILEY PERIODICALS, INC.

Entities:  

Keywords:  database; exome; genomic matchmaking; matchmaker exchange; phenotype

Mesh:

Year:  2015        PMID: 26239817     DOI: 10.1002/humu.22848

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  10 in total

1.  The Matchmaker Exchange: a platform for rare disease gene discovery.

Authors:  Anthony A Philippakis; Danielle R Azzariti; Sergi Beltran; Anthony J Brookes; Catherine A Brownstein; Michael Brudno; Han G Brunner; Orion J Buske; Knox Carey; Cassie Doll; Sergiu Dumitriu; Stephanie O M Dyke; Johan T den Dunnen; Helen V Firth; Richard A Gibbs; Marta Girdea; Michael Gonzalez; Melissa A Haendel; Ada Hamosh; Ingrid A Holm; Lijia Huang; Matthew E Hurles; Ben Hutton; Joel B Krier; Andriy Misyura; Christopher J Mungall; Justin Paschall; Benedict Paten; Peter N Robinson; François Schiettecatte; Nara L Sobreira; Ganesh J Swaminathan; Peter E Taschner; Sharon F Terry; Nicole L Washington; Stephan Züchner; Kym M Boycott; Heidi L Rehm
Journal:  Hum Mutat       Date:  2015-10       Impact factor: 4.878

2.  Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders.

Authors:  Michael H Guo; Andrew Dauber; Margaret F Lippincott; Yee-Ming Chan; Rany M Salem; Joel N Hirschhorn
Journal:  Am J Hum Genet       Date:  2016-08-18       Impact factor: 11.025

3.  Seven years since the launch of the Matchmaker Exchange: The evolution of genomic matchmaking.

Authors:  Kym M Boycott; Danielle R Azzariti; Ada Hamosh; Heidi L Rehm
Journal:  Hum Mutat       Date:  2022-05-10       Impact factor: 4.700

4.  When "N of 2" is not enough: integrating statistical and functional data in gene discovery.

Authors:  Christopher A Cassa; Sebastian Akle; Daniel M Jordan; Jill A Rosenfeld
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-05

5.  International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.

Authors:  Kym M Boycott; Ana Rath; Jessica X Chong; Taila Hartley; Fowzan S Alkuraya; Gareth Baynam; Anthony J Brookes; Michael Brudno; Angel Carracedo; Johan T den Dunnen; Stephanie O M Dyke; Xavier Estivill; Jack Goldblatt; Catherine Gonthier; Stephen C Groft; Ivo Gut; Ada Hamosh; Philip Hieter; Sophie Höhn; Matthew E Hurles; Petra Kaufmann; Bartha M Knoppers; Jeffrey P Krischer; Milan Macek; Gert Matthijs; Annie Olry; Samantha Parker; Justin Paschall; Anthony A Philippakis; Heidi L Rehm; Peter N Robinson; Pak-Chung Sham; Rumen Stefanov; Domenica Taruscio; Divya Unni; Megan R Vanstone; Feng Zhang; Han Brunner; Michael J Bamshad; Hanns Lochmüller
Journal:  Am J Hum Genet       Date:  2017-05-04       Impact factor: 11.025

6.  The role of the clinician in the multi-omics era: are you ready?

Authors:  Clara D M van Karnebeek; Saskia B Wortmann; Maja Tarailo-Graovac; Mirjam Langeveld; Carlos R Ferreira; Jiddeke M van de Kamp; Carla E Hollak; Wyeth W Wasserman; Hans R Waterham; Ron A Wevers; Tobias B Haack; Ronald J A Wanders; Kym M Boycott
Journal:  J Inherit Metab Dis       Date:  2018-01-23       Impact factor: 4.982

7.  Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative.

Authors:  Christoffer Nellåker; Fowzan S Alkuraya; Gareth Baynam; Raphael A Bernier; Francois P J Bernier; Vanessa Boulanger; Michael Brudno; Han G Brunner; Jill Clayton-Smith; Benjamin Cogné; Hugh J S Dawkins; Bert B A deVries; Sofia Douzgou; Tracy Dudding-Byth; Evan E Eichler; Michael Ferlaino; Karen Fieggen; Helen V Firth; David R FitzPatrick; Dylan Gration; Tudor Groza; Melissa Haendel; Nina Hallowell; Ada Hamosh; Jayne Hehir-Kwa; Marc-Phillip Hitz; Mark Hughes; Usha Kini; Tjitske Kleefstra; R Frank Kooy; Peter Krawitz; Sébastien Küry; Melissa Lees; Gholson J Lyon; Stanislas Lyonnet; Julien L Marcadier; Stephen Meyn; Veronika Moslerová; Juan M Politei; Cathryn C Poulton; F Lucy Raymond; Margot R F Reijnders; Peter N Robinson; Corrado Romano; Catherine M Rose; David C G Sainsbury; Lyn Schofield; Vernon R Sutton; Marek Turnovec; Anke Van Dijck; Hilde Van Esch; Andrew O M Wilkie
Journal:  Front Genet       Date:  2019-07-29       Impact factor: 4.599

8.  How to design a registry for undiagnosed patients in the framework of rare disease diagnosis: suggestions on software, data set and coding system.

Authors:  Alexandra Berger; Anne-Kathrin Rustemeier; Jens Göbel; Dennis Kadioglu; Vanessa Britz; Katharina Schubert; Klaus Mohnike; Holger Storf; Thomas O F Wagner
Journal:  Orphanet J Rare Dis       Date:  2021-05-01       Impact factor: 4.303

9.  De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome.

Authors:  Gerarda Cappuccio; Camille Sayou; Pauline Le Tanno; Emilie Tisserant; Ange-Line Bruel; Sara El Kennani; Joaquim Sá; Karen J Low; Cristina Dias; Markéta Havlovicová; Miroslava Hančárová; Evan E Eichler; Françoise Devillard; Sébastien Moutton; Julien Van-Gils; Christèle Dubourg; Sylvie Odent; Bénédicte Gerard; Amélie Piton; Toshiyuki Yamamoto; Nobuhiko Okamoto; Helen Firth; Kay Metcalfe; Anna Moh; Kimberly A Chapman; Erfan Aref-Eshghi; Jennifer Kerkhof; Annalaura Torella; Vincenzo Nigro; Laurence Perrin; Juliette Piard; Gwenaël Le Guyader; Thibaud Jouan; Christel Thauvin-Robinet; Yannis Duffourd; Jaya K George-Abraham; Catherine A Buchanan; Denise Williams; Usha Kini; Kate Wilson; Sérgio B Sousa; Raoul C M Hennekam; Bekim Sadikovic; Julien Thevenon; Jérôme Govin; Antonio Vitobello; Nicola Brunetti-Pierri
Journal:  Genet Med       Date:  2020-07-22       Impact factor: 8.822

10.  Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy.

Authors:  Jessica X Chong; Viviana Caputo; Ian G Phelps; Lorenzo Stella; Lisa Worgan; Jennifer C Dempsey; Alina Nguyen; Vincenzo Leuzzi; Richard Webster; Antonio Pizzuti; Colby T Marvin; Gisele E Ishak; Simone Ardern-Holmes; Zara Richmond; Michael J Bamshad; Xilma R Ortiz-Gonzalez; Marco Tartaglia; Maya Chopra; Dan Doherty
Journal:  Am J Hum Genet       Date:  2016-03-31       Impact factor: 11.043

  10 in total

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