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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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| Pubblicato in: | Nucleic Acids Res |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2017
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| Soggetti: | |
| Accesso online: | 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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