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Fast characterization of segmental duplications in genome assemblies
MOTIVATION: 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 wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129265/ https://www.ncbi.nlm.nih.gov/pubmed/30423092 http://dx.doi.org/10.1093/bioinformatics/bty586 |
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author | Numanagić, Ibrahim Gökkaya, Alim S Zhang, Lillian Berger, Bonnie Alkan, Can Hach, Faraz |
author_facet | Numanagić, Ibrahim Gökkaya, Alim S Zhang, Lillian Berger, Bonnie Alkan, Can Hach, Faraz |
author_sort | Numanagić, Ibrahim |
collection | PubMed |
description | MOTIVATION: 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. |
format | Online Article Text |
id | pubmed-6129265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61292652018-09-12 Fast characterization of segmental duplications in genome assemblies Numanagić, Ibrahim Gökkaya, Alim S Zhang, Lillian Berger, Bonnie Alkan, Can Hach, Faraz Bioinformatics Eccb 2018: European Conference on Computational Biology Proceedings MOTIVATION: 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. Oxford University Press 2018-09-01 2018-09-08 /pmc/articles/PMC6129265/ /pubmed/30423092 http://dx.doi.org/10.1093/bioinformatics/bty586 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Eccb 2018: European Conference on Computational Biology Proceedings Numanagić, Ibrahim Gökkaya, Alim S Zhang, Lillian Berger, Bonnie Alkan, Can Hach, Faraz Fast characterization of segmental duplications in genome assemblies |
title | Fast characterization of segmental duplications in genome assemblies |
title_full | Fast characterization of segmental duplications in genome assemblies |
title_fullStr | Fast characterization of segmental duplications in genome assemblies |
title_full_unstemmed | Fast characterization of segmental duplications in genome assemblies |
title_short | Fast characterization of segmental duplications in genome assemblies |
title_sort | fast characterization of segmental duplications in genome assemblies |
topic | Eccb 2018: European Conference on Computational Biology Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129265/ https://www.ncbi.nlm.nih.gov/pubmed/30423092 http://dx.doi.org/10.1093/bioinformatics/bty586 |
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