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• W2794682502 abstract "Prioritization of sequence variants for diagnosis and discovery of Mendelian diseases is challenging, especially in large collections of whole genome sequences (WGS). Fast, scalable solutions are needed for discovery research, for clinical applications, and for curation of massive public variant repositories such as dbSNP and gnomAD. In response, we have developed VVP, the VAAST Variant Prioritizer. VVP is ultrafast, scales to even the largest variant repositories and genome collections, and its outputs are designed to simplify clinical interpretation of variants of uncertain significance.We show that scoring the entire contents of dbSNP (> 155 million variants) requires only 95 min using a machine with 4 cpus and 16 GB of RAM, and that a 60X WGS can be processed in less than 5 min. We also demonstrate that VVP can score variants anywhere in the genome, regardless of type, effect, or location. It does so by integrating sequence conservation, the type of sequence change, allele frequencies, variant burden, and zygosity. Finally, we also show that VVP scores are consistently accurate, and easily interpreted, traits not shared by many commonly used tools such as SIFT and CADD.VVP provides rapid and scalable means to prioritize any sequence variant, anywhere in the genome, and its scores are designed to facilitate variant interpretation using ACMG and NHS guidelines. These traits make it well suited for operation on very large collections of WGS sequences." @default.
• W2794682502 created "2018-04-06" @default.
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• W2794682502 date "2018-02-20" @default.
• W2794682502 modified "2023-10-12" @default.
• W2794682502 title "The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool" @default.
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• W2794682502 doi "https://doi.org/10.1186/s12859-018-2056-y" @default.
• W2794682502 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5819680" @default.
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• W2794682502 hasPublicationYear "2018" @default.
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