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SMuRF: a novel tool to identify regulatory elements enriched for somatic point mutations
BACKGROUND: Single Nucleotide Variants (SNVs), including somatic point mutations and Single Nucleotide Polymorphisms (SNPs), in noncoding cis-regulatory elements (CREs) can affect gene regulation and lead to disease development. Several approaches have been developed to identify highly mutated regio...
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| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6258448/ https://ncbi.nlm.nih.gov/pubmed/30477433 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2501-y |
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