ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants.
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DOI: 10.1016/j.ajhg.2018.08.005
Abstract: Advances in high-throughput DNA sequencing have revolutionized the discovery of variants in the human genome; however, interpreting the phenotypic effects of those variants is still a challenge. While several computational approaches to predict variant impact… read more here.
Keywords: disease relevant; tool; disease; prediction ... See more keywords