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DEOGEN2: prediction and interactive visualization of single amino acid variant deleteriousness in human proteins
High-throughput sequencing methods are generating enormous amounts of genomic data, giving unprecedented insights into human genetic variation and its relation to disease. An individual human genome contains millions of Single Nucleotide Variants: to discriminate the deleterious from the benign ones...
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| Publicado no: | Nucleic Acids Res |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5570203/ https://ncbi.nlm.nih.gov/pubmed/28498993 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkx390 |
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