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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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| Yayımlandı: | Bioinformatics |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2016
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| 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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