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A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing
The genome of many species in the biosphere is a diploid consisting of paternal and maternal haplotypes. The differences between these two haplotypes range from single nucleotide polymorphisms (SNPs) to large-scale structural variations (SVs). Existing genome assemblers for next-generation sequencin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115803/ https://www.ncbi.nlm.nih.gov/pubmed/27861560 http://dx.doi.org/10.1371/journal.pone.0166721 |
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author | Ting, Chuan-Kang Lin, Choun-Sea Chan, Ming-Tsai Chen, Jian-Wei Chuang, Sheng-Yu Huang, Yao-Ting |
author_facet | Ting, Chuan-Kang Lin, Choun-Sea Chan, Ming-Tsai Chen, Jian-Wei Chuang, Sheng-Yu Huang, Yao-Ting |
author_sort | Ting, Chuan-Kang |
collection | PubMed |
description | The genome of many species in the biosphere is a diploid consisting of paternal and maternal haplotypes. The differences between these two haplotypes range from single nucleotide polymorphisms (SNPs) to large-scale structural variations (SVs). Existing genome assemblers for next-generation sequencing platforms attempt to reconstruct one consensus sequence, which is a mosaic of two parental haplotypes. Reconstructing paternal and maternal haplotypes is an important task in linkage analysis and association studies. This study designs and implemented HapSVAssembler on the basis of Genetic Algorithm (GA) and paired-end sequencing. The proposed method builds a consensus sequence, identifies various types of heterozygous variants, and reconstructs the paternal and maternal haplotypes by solving an optimization problem with a GA algorithm. Experimental results indicate that the HapSVAssembler has high accuracy and contiguity under various sequencing coverage, error rates, and insert sizes. The program is tested on pilot sequencing of a highly heterozygous genome, and 12,781 heterozygous SNPs and 602 hemizygous SVs are identified. We observe that, although the number of SVs is much less than that of SNPs, the genomic regions occupied by SVs are much larger, implying the heterozygosity computed using SNPs or k-mer spectrum may be under-estimated. |
format | Online Article Text |
id | pubmed-5115803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51158032016-12-08 A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing Ting, Chuan-Kang Lin, Choun-Sea Chan, Ming-Tsai Chen, Jian-Wei Chuang, Sheng-Yu Huang, Yao-Ting PLoS One Research Article The genome of many species in the biosphere is a diploid consisting of paternal and maternal haplotypes. The differences between these two haplotypes range from single nucleotide polymorphisms (SNPs) to large-scale structural variations (SVs). Existing genome assemblers for next-generation sequencing platforms attempt to reconstruct one consensus sequence, which is a mosaic of two parental haplotypes. Reconstructing paternal and maternal haplotypes is an important task in linkage analysis and association studies. This study designs and implemented HapSVAssembler on the basis of Genetic Algorithm (GA) and paired-end sequencing. The proposed method builds a consensus sequence, identifies various types of heterozygous variants, and reconstructs the paternal and maternal haplotypes by solving an optimization problem with a GA algorithm. Experimental results indicate that the HapSVAssembler has high accuracy and contiguity under various sequencing coverage, error rates, and insert sizes. The program is tested on pilot sequencing of a highly heterozygous genome, and 12,781 heterozygous SNPs and 602 hemizygous SVs are identified. We observe that, although the number of SVs is much less than that of SNPs, the genomic regions occupied by SVs are much larger, implying the heterozygosity computed using SNPs or k-mer spectrum may be under-estimated. Public Library of Science 2016-11-18 /pmc/articles/PMC5115803/ /pubmed/27861560 http://dx.doi.org/10.1371/journal.pone.0166721 Text en © 2016 Ting et al http://creativecommons.org/licenses/by/4.0/ 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ting, Chuan-Kang Lin, Choun-Sea Chan, Ming-Tsai Chen, Jian-Wei Chuang, Sheng-Yu Huang, Yao-Ting A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing |
title | A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing |
title_full | A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing |
title_fullStr | A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing |
title_full_unstemmed | A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing |
title_short | A Genetic Algorithm for Diploid Genome Reconstruction Using Paired-End Sequencing |
title_sort | genetic algorithm for diploid genome reconstruction using paired-end sequencing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115803/ https://www.ncbi.nlm.nih.gov/pubmed/27861560 http://dx.doi.org/10.1371/journal.pone.0166721 |
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