Literature DB >> 21778733

Copy number variation accuracy in genome-wide association studies.

Peng Lin1, Sarah M Hartz, Jen-Chyong Wang, Robert F Krueger, Tatiana M Foroud, Howard J Edenberg, John I Nurnberger, Andrew I Brooks, Jay A Tischfield, Laura Almasy, Bradley T Webb, Victor M Hesselbrock, Bernice Porjesz, Alison M Goate, Laura J Bierut, John P Rice.   

Abstract

BACKGROUND/AIM: Copy number variations (CNVs) are a major source of alterations among individuals and are a potential risk factor in many diseases. Numerous diseases have been linked to deletions and duplications of these chromosomal segments. Data from genome-wide association studies and other microarrays may be used to identify CNVs by several different computer programs, but the reliability of the results has been questioned.
METHODS: To help researchers reduce the number of false-positive CNVs that need to be followed up with laboratory testing, we evaluated the relative performance of CNVPartition, PennCNV and QuantiSNP, and developed a statistical method for estimating sensitivity and positive predictive values of CNV calls and tested it on 96 duplicate samples in our dataset.
RESULTS: We found that the positive predictive rate increases with the number of probes in the CNV and the size of the CNV, with the highest positive predicted rates in CNVs of at least 500 kb and at least 100 probes. Our analysis also indicates that identifying CNVs reported by multiple programs can greatly improve the reproducibility rate and the positive predicted rate.
CONCLUSION: Our methods can be used by investigators to identify CNVs in genome-wide data with greater reliability.
Copyright © 2011 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2011        PMID: 21778733      PMCID: PMC3153341          DOI: 10.1159/000324683

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  29 in total

1.  Detection of novel copy number variants in uterine leiomyomas using high-resolution SNP arrays.

Authors:  Wayne Bowden; Josh Skorupski; Ertug Kovanci; Aleksandar Rajkovic
Journal:  Mol Hum Reprod       Date:  2009-06-30       Impact factor: 4.025

2.  Copy number variation at 1q21.1 associated with neuroblastoma.

Authors:  Sharon J Diskin; Cuiping Hou; Joseph T Glessner; Edward F Attiyeh; Marci Laudenslager; Kristopher Bosse; Kristina Cole; Yaël P Mossé; Andrew Wood; Jill E Lynch; Katlyn Pecor; Maura Diamond; Cynthia Winter; Kai Wang; Cecilia Kim; Elizabeth A Geiger; Patrick W McGrady; Alexandra I F Blakemore; Wendy B London; Tamim H Shaikh; Jonathan Bradfield; Struan F A Grant; Hongzhe Li; Marcella Devoto; Eric R Rappaport; Hakon Hakonarson; John M Maris
Journal:  Nature       Date:  2009-06-18       Impact factor: 49.962

3.  A genome-wide association study of alcohol dependence.

Authors:  Laura J Bierut; Arpana Agrawal; Kathleen K Bucholz; Kimberly F Doheny; Cathy Laurie; Elizabeth Pugh; Sherri Fisher; Louis Fox; William Howells; Sarah Bertelsen; Anthony L Hinrichs; Laura Almasy; Naomi Breslau; Robert C Culverhouse; Danielle M Dick; Howard J Edenberg; Tatiana Foroud; Richard A Grucza; Dorothy Hatsukami; Victor Hesselbrock; Eric O Johnson; John Kramer; Robert F Krueger; Samuel Kuperman; Michael Lynskey; Karl Mann; Rosalind J Neuman; Markus M Nöthen; John I Nurnberger; Bernice Porjesz; Monika Ridinger; Nancy L Saccone; Scott F Saccone; Marc A Schuckit; Jay A Tischfield; Jen C Wang; Marcella Rietschel; Alison M Goate; John P Rice
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-02       Impact factor: 11.205

Review 4.  Comparing CNV detection methods for SNP arrays.

Authors:  Laura Winchester; Christopher Yau; Jiannis Ragoussis
Journal:  Brief Funct Genomic Proteomic       Date:  2009-09-08

5.  A new statistic to evaluate imputation reliability.

Authors:  Peng Lin; Sarah M Hartz; Zhehao Zhang; Scott F Saccone; Jia Wang; Jay A Tischfield; Howard J Edenberg; John R Kramer; Alison M Goate; Laura J Bierut; John P Rice
Journal:  PLoS One       Date:  2010-03-15       Impact factor: 3.240

6.  The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.

Authors:  Louise V Wain; Inti Pedroso; John E Landers; Gerome Breen; Christopher E Shaw; P Nigel Leigh; Robert H Brown; Martin D Tobin; Ammar Al-Chalabi
Journal:  PLoS One       Date:  2009-12-04       Impact factor: 3.240

7.  Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.

Authors:  Nick Craddock; Matthew E Hurles; Niall Cardin; Richard D Pearson; Vincent Plagnol; Samuel Robson; Damjan Vukcevic; Chris Barnes; Donald F Conrad; Eleni Giannoulatou; Chris Holmes; Jonathan L Marchini; Kathy Stirrups; Martin D Tobin; Louise V Wain; Chris Yau; Jan Aerts; Tariq Ahmad; T Daniel Andrews; Hazel Arbury; Anthony Attwood; Adam Auton; Stephen G Ball; Anthony J Balmforth; Jeffrey C Barrett; Inês Barroso; Anne Barton; Amanda J Bennett; Sanjeev Bhaskar; Katarzyna Blaszczyk; John Bowes; Oliver J Brand; Peter S Braund; Francesca Bredin; Gerome Breen; Morris J Brown; Ian N Bruce; Jaswinder Bull; Oliver S Burren; John Burton; Jake Byrnes; Sian Caesar; Chris M Clee; Alison J Coffey; John M C Connell; Jason D Cooper; Anna F Dominiczak; Kate Downes; Hazel E Drummond; Darshna Dudakia; Andrew Dunham; Bernadette Ebbs; Diana Eccles; Sarah Edkins; Cathryn Edwards; Anna Elliot; Paul Emery; David M Evans; Gareth Evans; Steve Eyre; Anne Farmer; I Nicol Ferrier; Lars Feuk; Tomas Fitzgerald; Edward Flynn; Alistair Forbes; Liz Forty; Jayne A Franklyn; Rachel M Freathy; Polly Gibbs; Paul Gilbert; Omer Gokumen; Katherine Gordon-Smith; Emma Gray; Elaine Green; Chris J Groves; Detelina Grozeva; Rhian Gwilliam; Anita Hall; Naomi Hammond; Matt Hardy; Pile Harrison; Neelam Hassanali; Husam Hebaishi; Sarah Hines; Anne Hinks; Graham A Hitman; Lynne Hocking; Eleanor Howard; Philip Howard; Joanna M M Howson; Debbie Hughes; Sarah Hunt; John D Isaacs; Mahim Jain; Derek P Jewell; Toby Johnson; Jennifer D Jolley; Ian R Jones; Lisa A Jones; George Kirov; Cordelia F Langford; Hana Lango-Allen; G Mark Lathrop; James Lee; Kate L Lee; Charlie Lees; Kevin Lewis; Cecilia M Lindgren; Meeta Maisuria-Armer; Julian Maller; John Mansfield; Paul Martin; Dunecan C O Massey; Wendy L McArdle; Peter McGuffin; Kirsten E McLay; Alex Mentzer; Michael L Mimmack; Ann E Morgan; Andrew P Morris; Craig Mowat; Simon Myers; William Newman; Elaine R Nimmo; Michael C O'Donovan; Abiodun Onipinla; Ifejinelo Onyiah; Nigel R Ovington; Michael J Owen; Kimmo Palin; Kirstie Parnell; David Pernet; John R B Perry; Anne Phillips; Dalila Pinto; Natalie J Prescott; Inga Prokopenko; Michael A Quail; Suzanne Rafelt; Nigel W Rayner; Richard Redon; David M Reid; Susan M Ring; Neil Robertson; Ellie Russell; David St Clair; Jennifer G Sambrook; Jeremy D Sanderson; Helen Schuilenburg; Carol E Scott; Richard Scott; Sheila Seal; Sue Shaw-Hawkins; Beverley M Shields; Matthew J Simmonds; Debbie J Smyth; Elilan Somaskantharajah; Katarina Spanova; Sophia Steer; Jonathan Stephens; Helen E Stevens; Millicent A Stone; Zhan Su; Deborah P M Symmons; John R Thompson; Wendy Thomson; Mary E Travers; Clare Turnbull; Armand Valsesia; Mark Walker; Neil M Walker; Chris Wallace; Margaret Warren-Perry; Nicholas A Watkins; John Webster; Michael N Weedon; Anthony G Wilson; Matthew Woodburn; B Paul Wordsworth; Allan H Young; Eleftheria Zeggini; Nigel P Carter; Timothy M Frayling; Charles Lee; Gil McVean; Patricia B Munroe; Aarno Palotie; Stephen J Sawcer; Stephen W Scherer; David P Strachan; Chris Tyler-Smith; Matthew A Brown; Paul R Burton; Mark J Caulfield; Alastair Compston; Martin Farrall; Stephen C L Gough; Alistair S Hall; Andrew T Hattersley; Adrian V S Hill; Christopher G Mathew; Marcus Pembrey; Jack Satsangi; Michael R Stratton; Jane Worthington; Panos Deloukas; Audrey Duncanson; Dominic P Kwiatkowski; Mark I McCarthy; Willem Ouwehand; Miles Parkes; Nazneen Rahman; John A Todd; Nilesh J Samani; Peter Donnelly
Journal:  Nature       Date:  2010-04-01       Impact factor: 49.962

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.  Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.

Authors:  Maja Bucan; Brett S Abrahams; Kai Wang; Joseph T Glessner; Edward I Herman; Lisa I Sonnenblick; Ana I Alvarez Retuerto; Marcin Imielinski; Dexter Hadley; Jonathan P Bradfield; Cecilia Kim; Nicole B Gidaya; Ingrid Lindquist; Ted Hutman; Marian Sigman; Vlad Kustanovich; Clara M Lajonchere; Andrew Singleton; Junhyong Kim; Thomas H Wassink; William M McMahon; Thomas Owley; John A Sweeney; Hilary Coon; John I Nurnberger; Mingyao Li; Rita M Cantor; Nancy J Minshew; James S Sutcliffe; Edwin H Cook; Geraldine Dawson; Joseph D Buxbaum; Struan F A Grant; Gerard D Schellenberg; Daniel H Geschwind; Hakon Hakonarson
Journal:  PLoS Genet       Date:  2009-06-26       Impact factor: 5.917

10.  Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.

Authors:  Jian Li; Tielin Yang; Liang Wang; Han Yan; Yinping Zhang; Yan Guo; Feng Pan; Zhixin Zhang; Yumei Peng; Qi Zhou; Lina He; Xuezhen Zhu; Hongyi Deng; Shawn Levy; Christopher J Papasian; Betty M Drees; James J Hamilton; Robert R Recker; Jing Cheng; Hong-Wen Deng
Journal:  PLoS One       Date:  2009-11-23       Impact factor: 3.240

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  11 in total

1.  Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence.

Authors:  Peng Lin; Sarah M Hartz; Jen-Chyong Wang; Arpana Agrawal; Tian-Xiao Zhang; Nicholas McKenna; Kathleen Bucholz; Andrew I Brooks; Jay A Tischfield; Howard J Edenberg; Victor M Hesselbrock; John R Kramer; Samuel Kuperman; Marc A Schuckit; Alison M Goate; Laura J Bierut; John P Rice
Journal:  Alcohol Clin Exp Res       Date:  2012-06-15       Impact factor: 3.455

2.  A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.

Authors:  C Fernandez-Rozadilla; J B Cazier; I Tomlinson; A Brea-Fernández; M J Lamas; M Baiget; L A López-Fernández; J Clofent; L Bujanda; D Gonzalez; L de Castro; K Hemminki; X Bessa; M Andreu; R Jover; R Xicola; X Llor; V Moreno; A Castells; S Castellví-Bel; A Carracedo; C Ruiz-Ponte
Journal:  Hum Genet       Date:  2013-11-12       Impact factor: 4.132

3.  The association of copy number variation and percent mammographic density.

Authors:  Elizabeth J Atkinson; Jeanette E Eckel-Passow; Alice Wang; Alexandra J Greenberg; Christopher G Scott; V Shane Pankratz; Kristen N Purrington; Thomas A Sellers; David N Rider; John A Heit; Mariza de Andrade; Julie M Cunningham; Fergus J Couch; Celine M Vachon
Journal:  BMC Res Notes       Date:  2015-07-08

4.  Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.

Authors:  Christina A Castellani; Melkaye G Melka; Andrea E Wishart; M Elizabeth O Locke; Zain Awamleh; Richard L O'Reilly; Shiva M Singh
Journal:  BMC Bioinformatics       Date:  2014-04-21       Impact factor: 3.169

5.  Identifying Potential Regions of Copy Number Variation for Bipolar Disorder.

Authors:  Yi-Hsuan Chen; Ru-Band Lu; Hung Hung; Po-Hsiu Kuo
Journal:  Microarrays (Basel)       Date:  2014-02-28

Review 6.  The Role of Constitutional Copy Number Variants in Breast Cancer.

Authors:  Logan C Walker; George A R Wiggins; John F Pearson
Journal:  Microarrays (Basel)       Date:  2015-09-08

7.  A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data.

Authors:  Ramakrishnan Rajagopalan; Jill R Murrell; Minjie Luo; Laura K Conlin
Journal:  Genome Med       Date:  2020-01-30       Impact factor: 11.117

8.  Detectable clonal mosaicism from birth to old age and its relationship to cancer.

Authors:  Cathy C Laurie; Cecelia A Laurie; Kenneth Rice; Kimberly F Doheny; Leila R Zelnick; Caitlin P McHugh; Hua Ling; Kurt N Hetrick; Elizabeth W Pugh; Chris Amos; Qingyi Wei; Li-e Wang; Jeffrey E Lee; Kathleen C Barnes; Nadia N Hansel; Rasika Mathias; Denise Daley; Terri H Beaty; Alan F Scott; Ingo Ruczinski; Rob B Scharpf; Laura J Bierut; Sarah M Hartz; Maria Teresa Landi; Neal D Freedman; Lynn R Goldin; David Ginsburg; Jun Li; Karl C Desch; Sara S Strom; William J Blot; Lisa B Signorello; Sue A Ingles; Stephen J Chanock; Sonja I Berndt; Loic Le Marchand; Brian E Henderson; Kristine R Monroe; John A Heit; Mariza de Andrade; Sebastian M Armasu; Cynthia Regnier; William L Lowe; M Geoffrey Hayes; Mary L Marazita; Eleanor Feingold; Jeffrey C Murray; Mads Melbye; Bjarke Feenstra; Jae H Kang; Janey L Wiggs; Gail P Jarvik; Andrew N McDavid; Venkatraman E Seshan; Daniel B Mirel; Andrew Crenshaw; Nataliya Sharopova; Anastasia Wise; Jess Shen; David R Crosslin; David M Levine; Xiuwen Zheng; Jenna I Udren; Siiri Bennett; Sarah C Nelson; Stephanie M Gogarten; Matthew P Conomos; Patrick Heagerty; Teri Manolio; Louis R Pasquale; Christopher A Haiman; Neil Caporaso; Bruce S Weir
Journal:  Nat Genet       Date:  2012-05-06       Impact factor: 38.330

9.  On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis.

Authors:  Roseann E Peterson; Hermine H Maes; Peng Lin; John R Kramer; Victor M Hesselbrock; Lance O Bauer; John I Nurnberger; Howard J Edenberg; Danielle M Dick; Bradley T Webb
Journal:  BMC Genomics       Date:  2014-05-14       Impact factor: 3.969

10.  A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer.

Authors:  Yajun Yu; Salem Werdyani; Megan Carey; Patrick Parfrey; Yildiz E Yilmaz; Sevtap Savas
Journal:  Mol Oncol       Date:  2021-08-05       Impact factor: 6.603

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