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dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Non-synonymous and Splice Site SNVs
The purpose of the dbNSFP is to provide a one-stop resource for functional predictions and annotations for human non-synonymous single-nucleotide variants (nsSNVs) and splice site variants (ssSNVs), and to facilitate the steps of filtering and prioritizing SNVs from a large list of SNVs discovered i...
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| Publicado no: | Hum Mutat |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4752381/ https://ncbi.nlm.nih.gov/pubmed/26555599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22932 |
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