Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels

BACKGROUND: RNA-sequencing (RNA-seq) is a powerful technique for the identification of genetic variants that affect gene-expression levels, either through expression quantitative trait locus (eQTL) mapping or through allele-specific expression (ASE) analysis. Given increasing numbers of RNA-seq samp...

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書誌詳細
出版年:Genome Med
主要な著者: Deelen, Patrick, Zhernakova, Daria V, de Haan, Mark, van der Sijde, Marijke, Bonder, Marc Jan, Karjalainen, Juha, van der Velde, K Joeri, Abbott, Kristin M, Fu, Jingyuan, Wijmenga, Cisca, Sinke, Richard J, Swertz, Morris A, Franke, Lude
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2015
主題:
Research
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4423486/
https://ncbi.nlm.nih.gov/pubmed/25954321
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-015-0152-4
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