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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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| Pubblicato in: | Bioinformatics |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2016
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| Soggetti: | |
| Accesso online: | 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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