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Comparing complex variants in family trios

MOTIVATION: 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...

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Detalles Bibliográficos
Autores principales: Toptaş, Berke Ç, Rakocevic, Goran, Kómár, Péter, Kural, Deniz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289131/
https://www.ncbi.nlm.nih.gov/pubmed/29868720
http://dx.doi.org/10.1093/bioinformatics/bty443
Descripción
Sumario:MOTIVATION: 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. RESULTS: 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. AVAILABILITY AND IMPLEMENTATION: 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 INFORMATION: Supplementary data are available at Bioinformatics online.