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      MetaSV: an accurate and integrative structural-variant caller for next generation sequencing

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          Abstract

          Summary: Structural variations (SVs) are large genomic rearrangements that vary significantly in size, making them challenging to detect with the relatively short reads from next-generation sequencing (NGS). Different SV detection methods have been developed; however, each is limited to specific kinds of SVs with varying accuracy and resolution. Previous works have attempted to combine different methods, but they still suffer from poor accuracy particularly for insertions. We propose MetaSV, an integrated SV caller which leverages multiple orthogonal SV signals for high accuracy and resolution. MetaSV proceeds by merging SVs from multiple tools for all types of SVs. It also analyzes soft-clipped reads from alignment to detect insertions accurately since existing tools underestimate insertion SVs. Local assembly in combination with dynamic programming is used to improve breakpoint resolution. Paired-end and coverage information is used to predict SV genotypes. Using simulation and experimental data, we demonstrate the effectiveness of MetaSV across various SV types and sizes.

          Availability and implementation: Code in Python is at http://bioinform.github.io/metasv/.

          Contact: rd@ 123456bina.com

          Supplementary information: Supplementary data are available at Bioinformatics online.

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          Most cited references7

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          Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library.

          Structural variants (SVs) are a major source of human genomic variation; however, characterizing them at nucleotide resolution remains challenging. Here we assemble a library of breakpoints at nucleotide resolution from collating and standardizing ~2,000 published SVs. For each breakpoint, we infer its ancestral state (through comparison to primate genomes) and its mechanism of formation (e.g., nonallelic homologous recombination, NAHR). We characterize breakpoint sequences with respect to genomic landmarks, chromosomal location, sequence motifs and physical properties, finding that the occurrence of insertions and deletions is more balanced than previously reported and that NAHR-formed breakpoints are associated with relatively rigid, stable DNA helices. Finally, we demonstrate an approach, BreakSeq, for scanning the reads from short-read sequenced genomes against our breakpoint library to accurately identify previously overlooked SVs, which we then validate by PCR. As new data become available, we expect our BreakSeq approach will become more sensitive and facilitate rapid SV genotyping of personal genomes.
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            Detecting and annotating genetic variations using the HugeSeq pipeline.

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              Enhanced structural variant and breakpoint detection using SVMerge by integration of multiple detection methods and local assembly

              We present a pipeline, SVMerge, to detect structural variants by integrating calls from several existing structural variant callers, which are then validated and the breakpoints refined using local de novo assembly. SVMerge is modular and extensible, allowing new callers to be incorporated as they become available. We applied SVMerge to the analysis of a HapMap trio, demonstrating enhanced structural variant detection, breakpoint refinement, and a lower false discovery rate. SVMerge can be downloaded from http://svmerge.sourceforge.net.
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                Author and article information

                Journal
                Bioinformatics
                Bioinformatics
                bioinformatics
                bioinfo
                Bioinformatics
                Oxford University Press
                1367-4803
                1367-4811
                15 August 2015
                10 April 2015
                10 April 2015
                : 31
                : 16
                : 2741-2744
                Affiliations
                1Bina Technologies, Roche Sequencing, Redwood City, CA 94065, USA,
                2Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06520, USA,
                3Department of Health Sciences Research, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA,
                4Department of Statistics, Stanford University, Stanford, CA 94035, USA and
                5Department of Health Research and Policy, Stanford University, Stanford, CA 94035, USA
                Author notes
                *To whom correspondence should be addressed.

                The authors wish it to be known that, in their opinion, the first two authors should be regarded as Joint First Authors.

                Associate Editor: Inanc Birol

                Article
                btv204
                10.1093/bioinformatics/btv204
                4528635
                25861968
                502abbe6-0bd3-4e0b-94ed-dbf3db807f4a
                © The Author 2015. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 December 2014
                : 27 March 2015
                : 07 April 2015
                Page count
                Pages: 4
                Categories
                Applications Notes
                Genome Analysis

                Bioinformatics & Computational biology
                Bioinformatics & Computational biology

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