| Literature DB >> 24413669 |
Glen Stecher1, Li Liu, Maxwell Sanderford, Daniel Peterson, Koichiro Tamura, Sudhir Kumar.
Abstract
Computational diagnosis of amino acid variants in the human exome is the first step in assessing the disruptive impacts of non-synonymous single nucleotide variants (nsSNVs) on human health and disease. The Molecular Evolutionary Genetics Analysis software with mutational diagnosis (MEGA-MD) is a suite of tools developed to forecast the deleteriousness of nsSNVs using multiple methods and to explore nsSNVs in the context of the variability permitted in the long-term evolution of the affected position. In its graphical interface for use on desktops, it enables interactive computational diagnosis and evolutionary exploration of nsSNVs. As a web service, MEGA-MD is suitable for diagnosing variants on an exome scale. The MEGA-MD suite intends to serve the needs for conducting low- and high-throughput analysis of nsSNVs in diverse applications.Entities:
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Year: 2014 PMID: 24413669 PMCID: PMC3998139 DOI: 10.1093/bioinformatics/btu018
Source DB: PubMed Journal: Bioinformatics ISSN: 1367-4803 Impact factor: 6.937