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PMID: 22876189 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.

PLoS genetics ·Vol. 8 ·No. 8 ·2012-00-00 ·Pages e1002793

Voight BF, Kang HM, Ding J, Palmer CD, Sidore C, Chines PS, Burtt NP, Fuchsberger C, Li Y, Erdmann J, Frayling TM, Heid IM, Jackson AU, Johnson T, Kilpeläinen TO, Lindgren CM, Morris AP, Prokopenko I, Randall JC, Saxena R, Soranzo N, Speliotes EK, Teslovich TM, Wheeler E, Maguire J, Parkin M, Potter S, Rayner NW, Robertson N, Stirrups K, Winckler W, Sanna S, Mulas A, Nagaraja R, Cucca F, Barroso I, Deloukas P, Loos RJ, Kathiresan S, Munroe PB, Newton-Cheh C, Pfeufer A, Samani NJ, Schunkert H, Hirschhorn JN, Altshuler D, McCarthy MI, Abecasis GR, Boehnke M

Abstract

Genome-wide association studies have identified hundreds of loci for type 2 diabetes, coronary artery disease and myocardial infarction, as well as for related traits such as body mass index, glucose and insulin levels, lipid levels, and blood pressure. These studies also have pointed to thousands of loci with promising but not yet compelling association evidence. To establish association at additional loci and to characterize the genome-wide significant loci by fine-mapping, we designed the "Metabochip," a custom genotyping array that assays nearly 200,000 SNP markers. Here, we describe the Metabochip and its component SNP sets, evaluate its performance in capturing variation across the allele-frequency spectrum, describe solutions to methodological challenges commonly encountered in its analysis, and evaluate its performance as a platform for genotype imputation. The metabochip achieves dramatic cost efficiencies compared to designing single-trait follow-up reagents, and provides the opportunity to compare results across a range of related traits. The metabochip and similar custom genotyping arrays offer a powerful and cost-effective approach to follow-up large-scale genotyping and sequencing studies and advance our understanding of the genetic basis of complex human diseases and traits.

MeSH Terms
Alleles Anthropometry/instrumentation,methods Cardiovascular Diseases/diagnosis,genetics,metabolism Diabetes Mellitus, Type 2/diagnosis,genetics,metabolism Gene Frequency Genome, Human Genome-Wide Association Study Genotype Genotyping Techniques Humans Metabolomics/instrumentation,methods Oligonucleotide Array Sequence Analysis/instrumentation,methods Phenotype Polymorphism, Single Nucleotide Quantitative Trait Loci
Authors & Affiliations
49 authors, click to expand affiliations / ORCID
Voight Benjamin F
Medical Population Genetics, The Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Kang Hyun Min
Ding Jun
Palmer Cameron D
Sidore Carlo
Chines Peter S
Burtt Noël P
Fuchsberger Christian
Li Yanming
Erdmann Jeanette
Frayling Timothy M
Heid Iris M
Jackson Anne U
Johnson Toby
Kilpeläinen Tuomas O
Lindgren Cecilia M
Morris Andrew P
Prokopenko Inga
Randall Joshua C
Saxena Richa
Soranzo Nicole
Speliotes Elizabeth K
Teslovich Tanya M
Wheeler Eleanor
Maguire Jared
Parkin Melissa
Potter Simon
Rayner N William
Robertson Neil
Stirrups Kathleen
Winckler Wendy
Sanna Serena
Mulas Antonella
Nagaraja Ramaiah
Cucca Francesco
Barroso Inês
Deloukas Panos
Loos Ruth J F
Kathiresan Sekar
Munroe Patricia B
Newton-Cheh Christopher
Pfeufer Arne
Samani Nilesh J
Schunkert Heribert
Hirschhorn Joel N
Altshuler David
McCarthy Mark I
Abecasis Gonçalo R
Boehnke Michael
Conflict of Interest

The authors have declared that no competing interests exist.

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Article Info
Journal
PLoS genetics
Abbr.
PLoS Genet
ISSN
1553-7404
Published
2012-00-00
Epub
2012-00-02
Pages
e1002793
Language
English
Region
United States
NLM ID
101239074
PMCID
PMC3410907
Subset
IM
Grants
NIDDK NIH HHS · R56 DK062370 · United States
NHGRI NIH HHS · U01 HG006513 · United States
NHGRI NIH HHS · U01 HG005214 · United States
NHGRI NIH HHS · R01 HG000376 · United States
NHGRI NIH HHS · T32 HG000040 · United States
NHGRI NIH HHS · R56 HG000376 · United States
NIDDK NIH HHS · R01 DK062370 · United States
Wellcome Trust · 090532 · United Kingdom
NHGRI NIH HHS · HG005581 · United States
NHGRI NIH HHS · RC2 HG005581 · United States
NIA NIH HHS · N01-AG-1-2109 · United States
British Heart Foundation · United Kingdom
Wellcome Trust · 064890 · United Kingdom
NIDDK NIH HHS · U01 DK062370 · United States
NIDDK NIH HHS · DK062370 · United States
NHGRI NIH HHS · HG005214 · United States
NIDDK NIH HHS · P30 DK020572 · United States
Wellcome Trust · United Kingdom
Medical Research Council · MC_U106188470 · United Kingdom
Wellcome Trust · 098051 · United Kingdom
Wellcome Trust · 081682 · United Kingdom
NHGRI NIH HHS · HG000376 · United States
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