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Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions
Copy-number variations (CNV), loss of heterozygosity (LOH), and uniparental disomy (UPD) are large genomic aberrations leading to many common inherited diseases, cancers, and other complex diseases. An integrated tool to identify these aberrations is essential in understanding diseases and in design...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412667/ https://www.ncbi.nlm.nih.gov/pubmed/25919136 http://dx.doi.org/10.1371/journal.pone.0123081 |
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author | Wang, Yu Li, Wei Xia, Yingying Wang, Chongzhi Tang, Y. Tom Guo, Wenying Li, Jinliang Zhao, Xia Sun, Yepeng Hu, Juan Zhen, Hefu Zhang, Xiandong Chen, Chao Shi, Yujian Li, Lin Cao, Hongzhi Du, Hongli Li, Jian |
author_facet | Wang, Yu Li, Wei Xia, Yingying Wang, Chongzhi Tang, Y. Tom Guo, Wenying Li, Jinliang Zhao, Xia Sun, Yepeng Hu, Juan Zhen, Hefu Zhang, Xiandong Chen, Chao Shi, Yujian Li, Lin Cao, Hongzhi Du, Hongli Li, Jian |
author_sort | Wang, Yu |
collection | PubMed |
description | Copy-number variations (CNV), loss of heterozygosity (LOH), and uniparental disomy (UPD) are large genomic aberrations leading to many common inherited diseases, cancers, and other complex diseases. An integrated tool to identify these aberrations is essential in understanding diseases and in designing clinical interventions. Previous discovery methods based on whole-genome sequencing (WGS) require very high depth of coverage on the whole genome scale, and are cost-wise inefficient. Another approach, whole exome genome sequencing (WEGS), is limited to discovering variations within exons. Thus, we are lacking efficient methods to detect genomic aberrations on the whole genome scale using next-generation sequencing technology. Here we present a method to identify genome-wide CNV, LOH and UPD for the human genome via selectively sequencing a small portion of genome termed Selected Target Regions (SeTRs). In our experiments, the SeTRs are covered by 99.73%~99.95% with sufficient depth. Our developed bioinformatics pipeline calls genome-wide CNVs with high confidence, revealing 8 credible events of LOH and 3 UPD events larger than 5M from 15 individual samples. We demonstrate that genome-wide CNV, LOH and UPD can be detected using a cost-effective SeTRs sequencing approach, and that LOH and UPD can be identified using just a sample grouping technique, without using a matched sample or familial information. |
format | Online Article Text |
id | pubmed-4412667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44126672015-05-12 Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions Wang, Yu Li, Wei Xia, Yingying Wang, Chongzhi Tang, Y. Tom Guo, Wenying Li, Jinliang Zhao, Xia Sun, Yepeng Hu, Juan Zhen, Hefu Zhang, Xiandong Chen, Chao Shi, Yujian Li, Lin Cao, Hongzhi Du, Hongli Li, Jian PLoS One Research Article Copy-number variations (CNV), loss of heterozygosity (LOH), and uniparental disomy (UPD) are large genomic aberrations leading to many common inherited diseases, cancers, and other complex diseases. An integrated tool to identify these aberrations is essential in understanding diseases and in designing clinical interventions. Previous discovery methods based on whole-genome sequencing (WGS) require very high depth of coverage on the whole genome scale, and are cost-wise inefficient. Another approach, whole exome genome sequencing (WEGS), is limited to discovering variations within exons. Thus, we are lacking efficient methods to detect genomic aberrations on the whole genome scale using next-generation sequencing technology. Here we present a method to identify genome-wide CNV, LOH and UPD for the human genome via selectively sequencing a small portion of genome termed Selected Target Regions (SeTRs). In our experiments, the SeTRs are covered by 99.73%~99.95% with sufficient depth. Our developed bioinformatics pipeline calls genome-wide CNVs with high confidence, revealing 8 credible events of LOH and 3 UPD events larger than 5M from 15 individual samples. We demonstrate that genome-wide CNV, LOH and UPD can be detected using a cost-effective SeTRs sequencing approach, and that LOH and UPD can be identified using just a sample grouping technique, without using a matched sample or familial information. Public Library of Science 2015-04-28 /pmc/articles/PMC4412667/ /pubmed/25919136 http://dx.doi.org/10.1371/journal.pone.0123081 Text en © 2015 Wang 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Yu Li, Wei Xia, Yingying Wang, Chongzhi Tang, Y. Tom Guo, Wenying Li, Jinliang Zhao, Xia Sun, Yepeng Hu, Juan Zhen, Hefu Zhang, Xiandong Chen, Chao Shi, Yujian Li, Lin Cao, Hongzhi Du, Hongli Li, Jian Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions |
title | Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions |
title_full | Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions |
title_fullStr | Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions |
title_full_unstemmed | Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions |
title_short | Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions |
title_sort | identifying human genome-wide cnv, loh and upd by targeted sequencing of selected regions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412667/ https://www.ncbi.nlm.nih.gov/pubmed/25919136 http://dx.doi.org/10.1371/journal.pone.0123081 |
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