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Localized structural frustration for evaluating the impact of sequence variants
Population-scale sequencing is increasingly uncovering large numbers of rare single-nucleotide variants (SNVs) in coding regions of the genome. The rarity of these variants makes it challenging to evaluate their deleteriousness with conventional phenotype–genotype associations. Protein structures pr...
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| Publicado no: | Nucleic Acids Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5137452/ https://ncbi.nlm.nih.gov/pubmed/27915290 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkw927 |
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