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Leveraging the Power of High Performance Computing for Next Generation Sequencing Data Analysis: Tricks and Twists from a High Throughput Exome Workflow

Author

Listed:
  • Amit Kawalia
  • Susanne Motameny
  • Stephan Wonczak
  • Holger Thiele
  • Lech Nieroda
  • Kamel Jabbari
  • Stefan Borowski
  • Vishal Sinha
  • Wilfried Gunia
  • Ulrich Lang
  • Viktor Achter
  • Peter Nürnberg

Abstract

Next generation sequencing (NGS) has been a great success and is now a standard method of research in the life sciences. With this technology, dozens of whole genomes or hundreds of exomes can be sequenced in rather short time, producing huge amounts of data. Complex bioinformatics analyses are required to turn these data into scientific findings. In order to run these analyses fast, automated workflows implemented on high performance computers are state of the art. While providing sufficient compute power and storage to meet the NGS data challenge, high performance computing (HPC) systems require special care when utilized for high throughput processing. This is especially true if the HPC system is shared by different users. Here, stability, robustness and maintainability are as important for automated workflows as speed and throughput. To achieve all of these aims, dedicated solutions have to be developed. In this paper, we present the tricks and twists that we utilized in the implementation of our exome data processing workflow. It may serve as a guideline for other high throughput data analysis projects using a similar infrastructure. The code implementing our solutions is provided in the supporting information files.

Suggested Citation

  • Amit Kawalia & Susanne Motameny & Stephan Wonczak & Holger Thiele & Lech Nieroda & Kamel Jabbari & Stefan Borowski & Vishal Sinha & Wilfried Gunia & Ulrich Lang & Viktor Achter & Peter Nürnberg, 2015. "Leveraging the Power of High Performance Computing for Next Generation Sequencing Data Analysis: Tricks and Twists from a High Throughput Exome Workflow," PLOS ONE, Public Library of Science, vol. 10(5), pages 1-16, May.
  • Handle: RePEc:plo:pone00:0126321
    DOI: 10.1371/journal.pone.0126321
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    Cited by:

    1. Azza E Ahmed & Jacob Heldenbrand & Yan Asmann & Faisal M Fadlelmola & Daniel S Katz & Katherine Kendig & Matthew C Kendzior & Tiffany Li & Yingxue Ren & Elliott Rodriguez & Matthew R Weber & Justin M , 2019. "Managing genomic variant calling workflows with Swift/T," PLOS ONE, Public Library of Science, vol. 14(7), pages 1-20, July.

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