1. PGen: large-scale genomic variations analysis workflow and browser in SoyKB
- Author
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Dong Xu, Shiyuan Chen, Shuai Zeng, Henry T. Nguyen, Babu Valliyodan, João Vitor Maldonado dos Santos, Nirav Merchant, Mats Rynge, Juexin Wang, Trupti Joshi, Yang Liu, Saad M. Khan, Yuanxun Zhang, and Prasad Calyam
- Subjects
0301 basic medicine ,Germplasm ,Computer science ,Data management ,Single-nucleotide polymorphism ,Genomics ,02 engineering and technology ,computer.software_genre ,Biochemistry ,Workflow ,03 medical and health sciences ,Structural Biology ,Genetic variation ,0202 electrical engineering, electronic engineering, information engineering ,Copy-number variation ,Molecular Biology ,2. Zero hunger ,Polymorphism, Genetic ,business.industry ,Applied Mathematics ,High-Throughput Nucleotide Sequencing ,020206 networking & telecommunications ,Sequence Analysis, DNA ,Computer Science Applications ,030104 developmental biology ,Proceedings ,Knowledge base ,Data analysis ,Data mining ,Soybeans ,DNA microarray ,business ,computer ,Cloud storage ,Workflow management system ,Genome, Plant ,Software - Abstract
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.
- Published
- 2016