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Matrix eQTL: ultra fast eQTL analysis via large matrix operations.
Shabalin, Andrey A.
Afiliação
  • Shabalin AA; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. shabalin@email.unc.edu
Bioinformatics ; 28(10): 1353-8, 2012 May 15.
Article em En | MEDLINE | ID: mdl-22492648
ABSTRACT
MOTIVATION Expression quantitative trait loci (eQTL) analysis links variations in gene expression levels to genotypes. For modern datasets, eQTL analysis is a computationally intensive task as it involves testing for association of billions of transcript-SNP (single-nucleotide polymorphism) pair. The heavy computational burden makes eQTL analysis less popular and sometimes forces analysts to restrict their attention to just a small subset of transcript-SNP pairs. As more transcripts and SNPs get interrogated over a growing number of samples, the demand for faster tools for eQTL analysis grows stronger.

RESULTS:

We have developed a new software for computationally efficient eQTL analysis called Matrix eQTL. In tests on large datasets, it was 2-3 orders of magnitude faster than existing popular tools for QTL/eQTL analysis, while finding the same eQTLs. The fast performance is achieved by special preprocessing and expressing the most computationally intensive part of the algorithm in terms of large matrix operations. Matrix eQTL supports additive linear and ANOVA models with covariates, including models with correlated and heteroskedastic errors. The issue of multiple testing is addressed by calculating false discovery rate; this can be done separately for cis- and trans-eQTLs.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Expressão Gênica / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Modelos Genéticos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Expressão Gênica / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Modelos Genéticos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Estados Unidos