4.7 Article

ViraPipe: scalable parallel pipeline for viral metagenome analysis from next generation sequencing reads

Journal

BIOINFORMATICS
Volume 34, Issue 6, Pages 928-935

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btx702

Keywords

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Funding

  1. Nordic Information for Action eScience Center (NIASC)
  2. Swedish strategic research foundation excellence project in biomarker research (BRIGHT)
  3. Academy of Finland project Advanced Parallel Testing and Verification Methods for Distributed Systems (APTV)
  4. Helsinki Institute for Information Technology program Foundations of Computational Health (FCHealth)

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Motivation: Next Generation Sequencing (NGS) technology enables identification of microbial genomes from massive amount of human microbiomes more rapidly and cheaper than ever before. However, the traditional sequential genome analysis algorithms, tools, and platforms are inefficient for performing large-scale metagenomic studies on ever-growing sample data volumes. Currently, there is an urgent need for scalable analysis pipelines that enable harnessing all the power of parallel computation in computing clusters and in cloud computing environments. We propose ViraPipe, a scalable metagenome analysis pipeline that is able to analyze thousands of human microbiomes in parallel in tolerable time. The pipeline is tuned for analyzing viral metagenomes and the software is applicable for other metagenomic analyses as well. ViraPipe integrates parallel BWA-MEM read aligner, MegaHit De novo assembler, and BLAST and HMMER3 sequence search tools. We show the scalability of ViraPipe by running experiments on mining virus related genomes from NGS datasets in a distributed Spark computing cluster. Results: ViraPipe analyses 768 human samples in 210 minutes on a Spark computing cluster comprising 23 nodes and 1288 cores in total. The speedup of ViraPipe executed on 23 nodes was 11x compared to the sequential analysis pipeline executed on a single node. The whole process includes parallel decompression, read interleaving, BWA-MEM read alignment, filtering and normalizing of non-human reads, De novo contigs assembling, and searching of sequences with BLAST and HMMER3 tools.

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