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GERV: a statistical method for generative evaluation of regulatory variants for transcription factor binding

Motivation: The majority of disease-associated variants identified in genome-wide association studies reside in noncoding regions of the genome with regulatory roles. Thus being able to interpret the functional consequence of a variant is essential for identifying causal variants in the analysis of...

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Detalhes bibliográficos
Publicado no:Bioinformatics
Main Authors: Zeng, Haoyang, Hashimoto, Tatsunori, Kang, Daniel D., Gifford, David K.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5860000/
https://ncbi.nlm.nih.gov/pubmed/26476779
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv565
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