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SNPhood: investigate, quantify and visualise the epigenomic neighbourhood of SNPs using NGS data

Motivation: The vast majority of the many thousands of disease-associated single nucleotide polymorphisms (SNPs) lie in the non-coding part of the genome. They are likely to affect regulatory elements, such as enhancers and promoters, rather than the function of a protein. To understand the molecula...

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Detaylı Bibliyografya
Yayımlandı:Bioinformatics
Asıl Yazarlar: Arnold, Christian, Bhat, Pooja, Zaugg, Judith B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4965630/
https://ncbi.nlm.nih.gov/pubmed/27153574
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw127
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