Fast characterization of segmental duplications in genome assemblies

buir.contributor.authorAlkan, Can
dc.citation.epagei714en_US
dc.citation.issueNumber17en_US
dc.citation.spagei706en_US
dc.citation.volumeNumber34en_US
dc.contributor.authorNumanagić, I.en_US
dc.contributor.authorGökkaya, Alim S.en_US
dc.contributor.authorZhang, L.en_US
dc.contributor.authorBerger, B.en_US
dc.contributor.authorAlkan, Canen_US
dc.contributor.authorHach, F.en_US
dc.date.accessioned2019-02-21T16:03:47Z
dc.date.available2019-02-21T16:03:47Z
dc.date.issued2018en_US
dc.departmentDepartment of Computer Engineeringen_US
dc.description.abstractMotivation Segmental duplications (SDs) or low-copy repeats, are segments of DNA > 1 Kbp with high sequence identity that are copied to other regions of the genome. SDs are among the most important sources of evolution, a common cause of genomic structural variation and several are associated with diseases of genomic origin including schizophrenia and autism. Despite their functional importance, SDs present one of the major hurdles for de novo genome assembly due to the ambiguity they cause in building and traversing both state-of-the-art overlap-layout-consensus and de Bruijn graphs. This causes SD regions to be misassembled, collapsed into a unique representation, or completely missing from assembled reference genomes for various organisms. In turn, this missing or incorrect information limits our ability to fully understand the evolution and the architecture of the genomes. Despite the essential need to accurately characterize SDs in assemblies, there has been only one tool that was developed for this purpose, called Whole-Genome Assembly Comparison (WGAC); its primary goal is SD detection. WGAC is comprised of several steps that employ different tools and custom scripts, which makes this strategy difficult and time consuming to use. Thus there is still a need for algorithms to characterize within-assembly SDs quickly, accurately, and in a user friendly manner. Results Here we introduce SEgmental Duplication Evaluation Framework (SEDEF) to rapidly detect SDs through sophisticated filtering strategies based on Jaccard similarity and local chaining. We show that SEDEF accurately detects SDs while maintaining substantial speed up over WGAC that translates into practical run times of minutes instead of weeks. Notably, our algorithm captures up to 25% 'pairwise error' between segments, whereas previous studies focused on only 10%, allowing us to more deeply track the evolutionary history of the genome. Availability and implementation SEDEF is available at https://github.com/vpc-ccg/sedef.
dc.description.provenanceMade available in DSpace on 2019-02-21T16:03:47Z (GMT). No. of bitstreams: 1 Bilkent-research-paper.pdf: 222869 bytes, checksum: 842af2b9bd649e7f548593affdbafbb3 (MD5) Previous issue date: 2018en
dc.description.sponsorshipThis work was supported in part by National Science and Engineering Research Council Discovery Grant to F.H., EMBO Installation Grant [IG-2521 to C.A.] and National Institutes of Health [grant GM108348 to B.B.].
dc.identifier.doi10.1093/bioinformatics/bty586
dc.identifier.issn1367-4803
dc.identifier.urihttp://hdl.handle.net/11693/50135
dc.language.isoEnglish
dc.publisherOxford University Press
dc.relation.isversionofhttps://doi.org/10.1093/bioinformatics/bty586
dc.relation.projectEMBO: IG-2521 - National Institutes of Health, NIH: GM108348 - Science and Engineering Research Council, SERC
dc.rightsinfo:eu-repo/semantics/openAccess
dc.source.titleBioinformaticsen_US
dc.titleFast characterization of segmental duplications in genome assembliesen_US
dc.typeArticleen_US

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