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PhD-SNP(g): a webserver and lightweight tool for scoring single nucleotide variants
One of the major challenges in human genetics is to identify functional effects of coding and non-coding single nucleotide variants (SNVs). In the past, several methods have been developed to identify disease-related single amino acid changes but only few tools are able to score the impact of non-co...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570245/ https://www.ncbi.nlm.nih.gov/pubmed/28482034 http://dx.doi.org/10.1093/nar/gkx369 |