Literature DB >> 25503493

A high-resolution copy-number variation resource for clinical and population genetics.

Mohammed Uddin1,2, Bhooma Thiruvahindrapuram1,2, Susan Walker1,2, Zhuozhi Wang1,2, Pingzhao Hu1,2, Sylvia Lamoureux1,2, John Wei1,2, Jeffrey R MacDonald1,2, Giovanna Pellecchia1,2, Chao Lu1,2, Anath C Lionel1,2, Matthew J Gazzellone1,2, John R McLaughlin3,4,5, Catherine Brown6, Irene L Andrulis5,7, Julia A Knight3,5, Jo-Anne Herbrick1,2, Richard F Wintle1,2, Peter Ray1,2,8, Dimitri J Stavropoulos8, Christian R Marshall1,2,8, Stephen W Scherer1,2,9.   

Abstract

PURPOSE: Chromosomal microarray analysis to assess copy-number variation has become a first-tier genetic diagnostic test for individuals with unexplained neurodevelopmental disorders or multiple congenital anomalies. More than 100 cytogenetic laboratories worldwide use the new ultra-high resolution Affymetrix CytoScan-HD array to genotype hundreds of thousands of samples per year. Our aim was to develop a copy-number variation resource from a new population sample that would enable more accurate interpretation of clinical genetics data on this microarray platform and others.
METHODS: Genotyping of 1,000 adult volunteers who are broadly representative of the Ontario population (as obtained from the Ontario Population Genomics Platform) was performed with the CytoScan-HD microarray system, which has 2.7 million probes. Four independent algorithms were applied to detect copy-number variations. Reproducibility and validation metrics were quantified using sample replicates and quantitative-polymerase chain reaction, respectively.
RESULTS: DNA from 873 individuals passed quality control and we identified 71,178 copy-number variations (81 copy-number variations/individual); 9.8% (6,984) of these copy-number variations were previously unreported. After applying three layers of filtering criteria, from our highest confidence copy-number variation data set we obtained >95% reproducibility and >90% validation rates (73% of these copy-number variations overlapped at least one gene).
CONCLUSION: The genotype data and annotated copy-number variations for this largely Caucasian population will represent a valuable public resource enabling clinical genetics research and diagnostics.

Entities:  

Mesh:

Year:  2014        PMID: 25503493      PMCID: PMC4752593          DOI: 10.1038/gim.2014.178

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  20 in total

Review 1.  Copy-number variations associated with neuropsychiatric conditions.

Authors:  Edwin H Cook; Stephen W Scherer
Journal:  Nature       Date:  2008-10-16       Impact factor: 49.962

Review 2.  Contemplating effects of genomic structural variation.

Authors:  Janet A Buchanan; Stephen W Scherer
Journal:  Genet Med       Date:  2008-09       Impact factor: 8.822

Review 3.  The clinical context of copy number variation in the human genome.

Authors:  Charles Lee; Stephen W Scherer
Journal:  Expert Rev Mol Med       Date:  2010-03-09       Impact factor: 5.600

4.  Integrating common and rare genetic variation in diverse human populations.

Authors:  David M Altshuler; Richard A Gibbs; Leena Peltonen; David M Altshuler; Richard A Gibbs; Leena Peltonen; Emmanouil Dermitzakis; Stephen F Schaffner; Fuli Yu; Leena Peltonen; Emmanouil Dermitzakis; Penelope E Bonnen; David M Altshuler; Richard A Gibbs; Paul I W de Bakker; Panos Deloukas; Stacey B Gabriel; Rhian Gwilliam; Sarah Hunt; Michael Inouye; Xiaoming Jia; Aarno Palotie; Melissa Parkin; Pamela Whittaker; Fuli Yu; Kyle Chang; Alicia Hawes; Lora R Lewis; Yanru Ren; David Wheeler; Richard A Gibbs; Donna Marie Muzny; Chris Barnes; Katayoon Darvishi; Matthew Hurles; Joshua M Korn; Kati Kristiansson; Charles Lee; Steven A McCarrol; James Nemesh; Emmanouil Dermitzakis; Alon Keinan; Stephen B Montgomery; Samuela Pollack; Alkes L Price; Nicole Soranzo; Penelope E Bonnen; Richard A Gibbs; Claudia Gonzaga-Jauregui; Alon Keinan; Alkes L Price; Fuli Yu; Verneri Anttila; Wendy Brodeur; Mark J Daly; Stephen Leslie; Gil McVean; Loukas Moutsianas; Huy Nguyen; Stephen F Schaffner; Qingrun Zhang; Mohammed J R Ghori; Ralph McGinnis; William McLaren; Samuela Pollack; Alkes L Price; Stephen F Schaffner; Fumihiko Takeuchi; Sharon R Grossman; Ilya Shlyakhter; Elizabeth B Hostetter; Pardis C Sabeti; Clement A Adebamowo; Morris W Foster; Deborah R Gordon; Julio Licinio; Maria Cristina Manca; Patricia A Marshall; Ichiro Matsuda; Duncan Ngare; Vivian Ota Wang; Deepa Reddy; Charles N Rotimi; Charmaine D Royal; Richard R Sharp; Changqing Zeng; Lisa D Brooks; Jean E McEwen
Journal:  Nature       Date:  2010-09-02       Impact factor: 49.962

5.  Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.

Authors:  Dalila Pinto; Katayoon Darvishi; Xinghua Shi; Diana Rajan; Diane Rigler; Tom Fitzgerald; Anath C Lionel; Bhooma Thiruvahindrapuram; Jeffrey R Macdonald; Ryan Mills; Aparna Prasad; Kristin Noonan; Susan Gribble; Elena Prigmore; Patricia K Donahoe; Richard S Smith; Ji Hyeon Park; Matthew E Hurles; Nigel P Carter; Charles Lee; Stephen W Scherer; Lars Feuk
Journal:  Nat Biotechnol       Date:  2011-05-08       Impact factor: 54.908

Review 6.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

7.  Ontario familial colon cancer registry: methods and first-year response rates.

Authors:  M Cotterchio; G McKeown-Eyssen; H Sutherland; G Buchan; M Aronson; A M Easson; J Macey; E Holowaty; S Gallinger
Journal:  Chronic Dis Can       Date:  2000

8.  Origins and functional impact of copy number variation in the human genome.

Authors:  Donald F Conrad; Dalila Pinto; Richard Redon; Lars Feuk; Omer Gokcumen; Yujun Zhang; Jan Aerts; T Daniel Andrews; Chris Barnes; Peter Campbell; Tomas Fitzgerald; Min Hu; Chun Hwa Ihm; Kati Kristiansson; Daniel G Macarthur; Jeffrey R Macdonald; Ifejinelo Onyiah; Andy Wing Chun Pang; Sam Robson; Kathy Stirrups; Armand Valsesia; Klaudia Walter; John Wei; Chris Tyler-Smith; Nigel P Carter; Charles Lee; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2009-10-07       Impact factor: 49.962

9.  Functional impact of global rare copy number variation in autism spectrum disorders.

Authors:  Dalila Pinto; Alistair T Pagnamenta; Lambertus Klei; Richard Anney; Daniele Merico; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S Abrahams; Joana Almeida; Elena Bacchelli; Gary D Bader; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Bölte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Susan E Bryson; Andrew R Carson; Guillermo Casallo; Jillian Casey; Brian H Y Chung; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Cheryl Cytrynbaum; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Andrew Green; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao-Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeff Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Marion Pilorge; Joseph Piven; Chris P Ponting; David J Posey; Annemarie Poustka; Fritz Poustka; Aparna Prasad; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Ana F Sequeira; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Inês Sousa; Olaf Stein; Nuala Sykes; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Wang; Thomas H Wassink; Caleb Webber; Rosanna Weksberg; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Jing Wu; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Joseph D Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael L Cuccaro; Bernie Devlin; Sean Ennis; Louise Gallagher; Daniel H Geschwind; Michael Gill; Jonathan L Haines; Joachim Hallmayer; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret A Pericak-Vance; Gerard D Schellenberg; Peter Szatmari; Astrid M Vicente; Veronica J Vieland; Ellen M Wijsman; Stephen W Scherer; James S Sutcliffe; Catalina Betancur
Journal:  Nature       Date:  2010-06-09       Impact factor: 49.962

10.  Clinical genetic testing for patients with autism spectrum disorders.

Authors:  Yiping Shen; Kira A Dies; Ingrid A Holm; Carolyn Bridgemohan; Magdi M Sobeih; Elizabeth B Caronna; Karen J Miller; Jean A Frazier; Iris Silverstein; Jonathan Picker; Laura Weissman; Peter Raffalli; Shafali Jeste; Laurie A Demmer; Heather K Peters; Stephanie J Brewster; Sara J Kowalczyk; Beth Rosen-Sheidley; Caroline McGowan; Andrew W Duda; Sharyn A Lincoln; Kathryn R Lowe; Alison Schonwald; Michael Robbins; Fuki Hisama; Robert Wolff; Ronald Becker; Ramzi Nasir; David K Urion; Jeff M Milunsky; Leonard Rappaport; James F Gusella; Christopher A Walsh; Bai-Lin Wu; David T Miller
Journal:  Pediatrics       Date:  2010-03-15       Impact factor: 7.124

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  36 in total

1.  Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis.

Authors:  Bo Zhou; Steve S Ho; Xianglong Zhang; Reenal Pattni; Rajini R Haraksingh; Alexander E Urban
Journal:  J Med Genet       Date:  2018-07-30       Impact factor: 6.318

2.  Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.

Authors:  Tamar Harel; Wan Hee Yoon; Caterina Garone; Shen Gu; Zeynep Coban-Akdemir; Mohammad K Eldomery; Jennifer E Posey; Shalini N Jhangiani; Jill A Rosenfeld; Megan T Cho; Stephanie Fox; Marjorie Withers; Stephanie M Brooks; Theodore Chiang; Lita Duraine; Serkan Erdin; Bo Yuan; Yunru Shao; Elie Moussallem; Costanza Lamperti; Maria A Donati; Joshua D Smith; Heather M McLaughlin; Christine M Eng; Magdalena Walkiewicz; Fan Xia; Tommaso Pippucci; Pamela Magini; Marco Seri; Massimo Zeviani; Michio Hirano; Jill V Hunter; Myriam Srour; Stefano Zanigni; Richard Alan Lewis; Donna M Muzny; Timothy E Lotze; Eric Boerwinkle; Richard A Gibbs; Scott E Hickey; Brett H Graham; Yaping Yang; Daniela Buhas; Donna M Martin; Lorraine Potocki; Claudio Graziano; Hugo J Bellen; James R Lupski
Journal:  Am J Hum Genet       Date:  2016-09-15       Impact factor: 11.025

3.  DNA copy number profiling in microsatellite-stable and microsatellite-unstable hereditary non-polyposis colorectal cancers by targeted CNV array.

Authors:  Weixiang Chen; Jun Ding; Long Jiang; Zebing Liu; Xiaoyan Zhou; Daren Shi
Journal:  Funct Integr Genomics       Date:  2016-11-28       Impact factor: 3.410

4.  A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.

Authors:  Brett Trost; Susan Walker; Zhuozhi Wang; Bhooma Thiruvahindrapuram; Jeffrey R MacDonald; Wilson W L Sung; Sergio L Pereira; Joe Whitney; Ada J S Chan; Giovanna Pellecchia; Miriam S Reuter; Si Lok; Ryan K C Yuen; Christian R Marshall; Daniele Merico; Stephen W Scherer
Journal:  Am J Hum Genet       Date:  2018-01-04       Impact factor: 11.025

5.  Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.

Authors:  Zeynep Yilmaz; Jin P Szatkiewicz; James J Crowley; NaEshia Ancalade; Marek K Brandys; Annemarie van Elburg; Carolien G F de Kovel; Roger A H Adan; Anke Hinney; Johannes Hebebrand; Monica Gratacos; Fernando Fernandez-Aranda; Georgia Escaramis; Juan R Gonzalez; Xavier Estivill; Eleftheria Zeggini; Patrick F Sullivan; Cynthia M Bulik
Journal:  Psychiatr Genet       Date:  2017-08       Impact factor: 2.458

6.  Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans.

Authors:  Lisa A Lansdon; Benjamin W Darbro; Aline L Petrin; Alissa M Hulstrand; Jennifer M Standley; Rachel B Brouillette; Abby Long; M Adela Mansilla; Robert A Cornell; Jeffrey C Murray; Douglas W Houston; J Robert Manak
Journal:  Genetics       Date:  2017-11-21       Impact factor: 4.562

7.  affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling.

Authors:  Carles Hernandez-Ferrer; Ines Quintela Garcia; Katharina Danielski; Ángel Carracedo; Luis A Pérez-Jurado; Juan R González
Journal:  BMC Bioinformatics       Date:  2015-05-20       Impact factor: 3.169

8.  Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients.

Authors:  Nancy Choucair; Joelle Abou Ghoch; Sandra Corbani; Pierre Cacciagli; Cecile Mignon-Ravix; Nabiha Salem; Nadine Jalkh; Sandra El Sabbagh; Ali Fawaz; Tony Ibrahim; Laurent Villard; André Mégarbané; Eliane Chouery
Journal:  Mol Cytogenet       Date:  2015-04-09       Impact factor: 2.009

9.  Annexin A8 identifies a subpopulation of transiently quiescent c-kit positive luminal progenitor cells of the ductal mammary epithelium.

Authors:  Juan Manuel Iglesias; Claire J Cairney; Roderick K Ferrier; Laura McDonald; Kelly Soady; Howard Kendrick; Marie-Anne Pringle; Reginald O Morgan; Finian Martin; Matthew J Smalley; Karen Blyth; Torsten Stein
Journal:  PLoS One       Date:  2015-03-24       Impact factor: 3.240

10.  Clinically relevant copy number variations detected in cerebral palsy.

Authors:  Maryam Oskoui; Matthew J Gazzellone; Bhooma Thiruvahindrapuram; Mehdi Zarrei; John Andersen; John Wei; Zhuozhi Wang; Richard F Wintle; Christian R Marshall; Ronald D Cohn; Rosanna Weksberg; Dimitri J Stavropoulos; Darcy Fehlings; Michael I Shevell; Stephen W Scherer
Journal:  Nat Commun       Date:  2015-08-03       Impact factor: 14.919

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