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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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Bibliografiske detaljer
Udgivet i:Nucleic Acids Res
Main Authors: Raimondi, Daniele, Tanyalcin, Ibrahim, Ferté, Julien, Gazzo, Andrea, Orlando, Gabriele, Lenaerts, Tom, Rooman, Marianne, Vranken, Wim
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2017
Fag:
Online adgang: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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