{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,26]],"date-time":"2026-02-26T20:34:49Z","timestamp":1772138089637,"version":"3.50.1"},"reference-count":23,"publisher":"Oxford University Press (OUP)","issue":"24","license":[{"start":{"date-parts":[[2018,6,1]],"date-time":"2018-06-01T00:00:00Z","timestamp":1527811200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100000276","name":"UK Department of Health","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100000276","id-type":"DOI","asserted-by":"crossref"}]},{"name":"SBRI Genomics Competition: Enabling Technologies for Genomic Sequence Data Analysis and Interpretation"},{"name":"Genomics England"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,12,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Motivation<\/jats:title>\n                    <jats:p>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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Availability and implementation<\/jats:title>\n                    <jats:p>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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Supplementary information<\/jats:title>\n                    <jats:p>Supplementary data are available at Bioinformatics online.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1093\/bioinformatics\/bty443","type":"journal-article","created":{"date-parts":[[2018,5,29]],"date-time":"2018-05-29T15:12:41Z","timestamp":1527606761000},"page":"4241-4247","source":"Crossref","is-referenced-by-count":10,"title":["Comparing complex variants in family trios"],"prefix":"10.1093","volume":"34","author":[{"given":"Berke \u00c7","family":"Topta\u015f","sequence":"first","affiliation":[{"name":"R&D Seven Bridges Genomics, Cambridge, MA, USA"},{"name":"R&D Totient, Cambridge, MA, USA"}]},{"given":"Goran","family":"Rakocevic","sequence":"additional","affiliation":[{"name":"R&D Seven Bridges Genomics, Cambridge, MA, USA"},{"name":"R&D Totient, Cambridge, MA, USA"}]},{"given":"P\u00e9ter","family":"K\u00f3m\u00e1r","sequence":"additional","affiliation":[{"name":"R&D Seven Bridges Genomics, Cambridge, MA, USA"},{"name":"R&D Totient, Cambridge, MA, USA"}]},{"given":"Deniz","family":"Kural","sequence":"additional","affiliation":[{"name":"R&D Seven Bridges Genomics, Cambridge, MA, USA"},{"name":"R&D Totient, Cambridge, MA, USA"}]}],"member":"286","published-online":{"date-parts":[[2018,6,1]]},"reference":[{"key":"2023012712244308900_bty443-B1","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1038\/nature15393","article-title":"A global reference for human genetic variation","volume":"526","author":"Genome Project Consortium","year":"2015","journal-title":"Nature"},{"key":"2023012712244308900_bty443-B2","article-title":"Comparing variant call files for performance benchmarking of next-generation sequencing variant calling pipelines","author":"Cleary","year":"2015","journal-title":"bioRxiv"},{"key":"2023012712244308900_bty443-B3","doi-asserted-by":"crossref","first-page":"712","DOI":"10.1038\/ng.862","article-title":"Variation in genome-wide mutation rates within and between human families","volume":"43","author":"Conrad","year":"2011","journal-title":"Nat. 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