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PGen: large-scale genomic variations analysis workflow and browser in SoyKB
BACKGROUND: With the advances in next-generation sequencing (NGS) technology and significant reductions in sequencing costs, it is now possible to sequence large collections of germplasm in crops for detecting genome-scale genetic variations and to apply the knowledge towards improvements in traits....
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074001/ https://www.ncbi.nlm.nih.gov/pubmed/27766951 http://dx.doi.org/10.1186/s12859-016-1227-y |
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author | Liu, Yang Khan, Saad M. Wang, Juexin Rynge, Mats Zhang, Yuanxun Zeng, Shuai Chen, Shiyuan Maldonado dos Santos, Joao V. Valliyodan, Babu Calyam, Prasad P. Merchant, Nirav Nguyen, Henry T. Xu, Dong Joshi, Trupti |
author_facet | Liu, Yang Khan, Saad M. Wang, Juexin Rynge, Mats Zhang, Yuanxun Zeng, Shuai Chen, Shiyuan Maldonado dos Santos, Joao V. Valliyodan, Babu Calyam, Prasad P. Merchant, Nirav Nguyen, Henry T. Xu, Dong Joshi, Trupti |
author_sort | Liu, Yang |
collection | PubMed |
description | BACKGROUND: With the advances in next-generation sequencing (NGS) technology and significant reductions in sequencing costs, it is now possible to sequence large collections of germplasm in crops for detecting genome-scale genetic variations and to apply the knowledge towards improvements in traits. To efficiently facilitate large-scale NGS resequencing data analysis of genomic variations, we have developed “PGen”, an integrated and optimized workflow using the Extreme Science and Engineering Discovery Environment (XSEDE) high-performance computing (HPC) virtual system, iPlant cloud data storage resources and Pegasus workflow management system (Pegasus-WMS). The workflow allows users to identify single nucleotide polymorphisms (SNPs) and insertion-deletions (indels), perform SNP annotations and conduct copy number variation analyses on multiple resequencing datasets in a user-friendly and seamless way. RESULTS: We have developed both a Linux version in GitHub (https://github.com/pegasus-isi/PGen-GenomicVariations-Workflow) and a web-based implementation of the PGen workflow integrated within the Soybean Knowledge Base (SoyKB), (http://soykb.org/Pegasus/index.php). Using PGen, we identified 10,218,140 single-nucleotide polymorphisms (SNPs) and 1,398,982 indels from analysis of 106 soybean lines sequenced at 15X coverage. 297,245 non-synonymous SNPs and 3330 copy number variation (CNV) regions were identified from this analysis. SNPs identified using PGen from additional soybean resequencing projects adding to 500+ soybean germplasm lines in total have been integrated. These SNPs are being utilized for trait improvement using genotype to phenotype prediction approaches developed in-house. In order to browse and access NGS data easily, we have also developed an NGS resequencing data browser (http://soykb.org/NGS_Resequence/NGS_index.php) within SoyKB to provide easy access to SNP and downstream analysis results for soybean researchers. CONCLUSION: PGen workflow has been optimized for the most efficient analysis of soybean data using thorough testing and validation. This research serves as an example of best practices for development of genomics data analysis workflows by integrating remote HPC resources and efficient data management with ease of use for biological users. PGen workflow can also be easily customized for analysis of data in other species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1227-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5074001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50740012016-10-27 PGen: large-scale genomic variations analysis workflow and browser in SoyKB Liu, Yang Khan, Saad M. Wang, Juexin Rynge, Mats Zhang, Yuanxun Zeng, Shuai Chen, Shiyuan Maldonado dos Santos, Joao V. Valliyodan, Babu Calyam, Prasad P. Merchant, Nirav Nguyen, Henry T. Xu, Dong Joshi, Trupti BMC Bioinformatics Proceedings BACKGROUND: With the advances in next-generation sequencing (NGS) technology and significant reductions in sequencing costs, it is now possible to sequence large collections of germplasm in crops for detecting genome-scale genetic variations and to apply the knowledge towards improvements in traits. To efficiently facilitate large-scale NGS resequencing data analysis of genomic variations, we have developed “PGen”, an integrated and optimized workflow using the Extreme Science and Engineering Discovery Environment (XSEDE) high-performance computing (HPC) virtual system, iPlant cloud data storage resources and Pegasus workflow management system (Pegasus-WMS). The workflow allows users to identify single nucleotide polymorphisms (SNPs) and insertion-deletions (indels), perform SNP annotations and conduct copy number variation analyses on multiple resequencing datasets in a user-friendly and seamless way. RESULTS: We have developed both a Linux version in GitHub (https://github.com/pegasus-isi/PGen-GenomicVariations-Workflow) and a web-based implementation of the PGen workflow integrated within the Soybean Knowledge Base (SoyKB), (http://soykb.org/Pegasus/index.php). Using PGen, we identified 10,218,140 single-nucleotide polymorphisms (SNPs) and 1,398,982 indels from analysis of 106 soybean lines sequenced at 15X coverage. 297,245 non-synonymous SNPs and 3330 copy number variation (CNV) regions were identified from this analysis. SNPs identified using PGen from additional soybean resequencing projects adding to 500+ soybean germplasm lines in total have been integrated. These SNPs are being utilized for trait improvement using genotype to phenotype prediction approaches developed in-house. In order to browse and access NGS data easily, we have also developed an NGS resequencing data browser (http://soykb.org/NGS_Resequence/NGS_index.php) within SoyKB to provide easy access to SNP and downstream analysis results for soybean researchers. CONCLUSION: PGen workflow has been optimized for the most efficient analysis of soybean data using thorough testing and validation. This research serves as an example of best practices for development of genomics data analysis workflows by integrating remote HPC resources and efficient data management with ease of use for biological users. PGen workflow can also be easily customized for analysis of data in other species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1227-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-06 /pmc/articles/PMC5074001/ /pubmed/27766951 http://dx.doi.org/10.1186/s12859-016-1227-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Proceedings Liu, Yang Khan, Saad M. Wang, Juexin Rynge, Mats Zhang, Yuanxun Zeng, Shuai Chen, Shiyuan Maldonado dos Santos, Joao V. Valliyodan, Babu Calyam, Prasad P. Merchant, Nirav Nguyen, Henry T. Xu, Dong Joshi, Trupti PGen: large-scale genomic variations analysis workflow and browser in SoyKB |
title | PGen: large-scale genomic variations analysis workflow and browser in SoyKB |
title_full | PGen: large-scale genomic variations analysis workflow and browser in SoyKB |
title_fullStr | PGen: large-scale genomic variations analysis workflow and browser in SoyKB |
title_full_unstemmed | PGen: large-scale genomic variations analysis workflow and browser in SoyKB |
title_short | PGen: large-scale genomic variations analysis workflow and browser in SoyKB |
title_sort | pgen: large-scale genomic variations analysis workflow and browser in soykb |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074001/ https://www.ncbi.nlm.nih.gov/pubmed/27766951 http://dx.doi.org/10.1186/s12859-016-1227-y |
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