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Improving the Assessment of the Outcome of Nonsynonymous SNVs with a Consensus Deleteriousness Score, Condel
Several large ongoing initiatives that profit from next-generation sequencing technologies have driven—and in coming years will continue to drive—the emergence of long catalogs of missense single-nucleotide variants (SNVs) in the human genome. As a consequence, researchers have developed various met...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3071923/ https://ncbi.nlm.nih.gov/pubmed/21457909 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2011.03.004 |
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