{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,26]],"date-time":"2026-03-26T08:28:18Z","timestamp":1774513698730,"version":"3.50.1"},"reference-count":59,"publisher":"Oxford University Press (OUP)","issue":"12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2014,6,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Motivation: Advances in sequencing technologies and computational algorithms have enabled the study of genomic variants to dissect their functional consequence. Despite this unprecedented progress, current tools fail to reliably detect and characterize more complex allelic variants, such as short tandem repeats (STRs). We developed TSSV as an efficient and sensitive tool to specifically profile all allelic variants present in targeted loci. Based on its design, requiring only two short flanking sequences, TSSV can work without the use of a complete reference sequence to reliably profile highly polymorphic, repetitive or uncharacterized regions.<\/jats:p>\n               <jats:p>Results: We show that TSSV can accurately determine allelic STR structures in mixtures with 10% representation of minor alleles or complex mixtures in which a single STR allele is shared. Furthermore, we show the universal utility of TSSV in two other independent studies: characterizing de novo mutations introduced by transcription activator-like effector nucleases (TALENs) and profiling the noise and systematic errors in an IonTorrent sequencing experiment. TSSV complements the existing tools by aiding the study of highly polymorphic and complex regions and provides a high-resolution map that can be used in a wide range of applications, from personal genomics to forensic analysis and clinical diagnostics.<\/jats:p>\n               <jats:p>Availability and implementation: We have implemented TSSV as a Python package that can be installed through the command-line using pip install TSSV command. Its source code and documentation are available at https:\/\/pypi.python.org\/pypi\/tssv and http:\/\/www.lgtc.nl\/tssv.<\/jats:p>\n               <jats:p>Contact: \u00a0S.Y.Anvar@lumc.nl<\/jats:p>\n               <jats:p>Supplementary information: \u00a0Supplementary data are available at Bioinformatics online.<\/jats:p>","DOI":"10.1093\/bioinformatics\/btu068","type":"journal-article","created":{"date-parts":[[2014,2,15]],"date-time":"2014-02-15T02:04:22Z","timestamp":1392429862000},"page":"1651-1659","source":"Crossref","is-referenced-by-count":45,"title":["TSSV: a tool for characterization of complex allelic variants in pure and mixed genomes"],"prefix":"10.1093","volume":"30","author":[{"given":"Seyed Yahya","family":"Anvar","sequence":"first","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"},{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Kristiaan J.","family":"van der Gaag","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Jaap W. F.","family":"van der Heijden","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Marcel H. A. M.","family":"Veltrop","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Rolf H. A. M.","family":"Vossen","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Rick H.","family":"de Leeuw","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Cor","family":"Breukel","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Henk P. J.","family":"Buermans","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"},{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"J. Sjef","family":"Verbeek","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Peter","family":"de Knijff","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Johan T.","family":"den Dunnen","sequence":"additional","affiliation":[{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"},{"name":"1 Department of Human Genetic, 2Leiden Genome Technology Center, Leiden University Medical Center, Leiden, 2300 RC, The Netherlands and 3Netherlands Bioinformatics Centre, Leiden, The Netherlands"}]},{"given":"Jeroen F. 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