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Variant Set Enrichment: an R package to identify disease-associated functional genomic regions

BACKGROUND: Genetic predispositions to diseases populate the noncoding regions of the human genome. Delineating their functional basis can inform on the mechanisms contributing to disease development. However, this remains a challenge due to the poor characterization of the noncoding genome. Here, w...

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書目詳細資料
發表在:BioData Min
Main Authors: Ahmed, Musaddeque, Sallari, Richard C., Guo, Haiyang, Moore, Jason H., He, Housheng Hansen, Lupien, Mathieu
格式: Artigo
語言:Inglês
出版: BioMed Central 2017
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5320724/
https://ncbi.nlm.nih.gov/pubmed/28239419
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13040-017-0129-5
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