Comparing complex variants in family trios.
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Where this comes from
- Record sourced from PubMed, PMID 29868720.
- Also identified by DOI 10.1093/bioinformatics/bty443 and PMC identifier 6289131.
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Abstract
Several tools exist to count Mendelian violations in family trios by comparing variants at the same genomic positions. This naive variant comparison, however, fails to assess regions where multiple variants need to be examined together, resulting in reduced accuracy of existing Mendelian violation checking tools. We introduce VBT, a trio concordance analysis tool, which identifies Mendelian violations by approximately solving the 3-way variant matching problem to resolve variant representation differences in family trios. We show that VBT outperforms previous trio comparison methods by accuracy. VBT is implemented in C++ and source code is available under GNU GPLv3 license at the following URL: https://github.com/sbg/VBT-TrioAnalysis.git. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genome
- Genomics
- Software