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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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| Publié dans: | Bioinformatics |
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| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Oxford University Press
2016
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| Sujets: | |
| Accès en ligne: | 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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