PEMapper and PECaller provide a simplified approach to whole-genome sequencing

International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

The analysis of human whole-genome sequencing data presents significant computational challenges. The sheer size of datasets places an enormous burden on computational, disk array, and network resources. Here, we present an integrated computational package, PEMapper/PECaller, that was designed specifically to minimize the burden on networks and disk arrays, create output files that are minimal in size, and run in a highly computationally efficient way, with the single goal of enabling whole-genome sequencing at scale. In addition to improved computational efficiency, we implement a statistical framework that allows for a base by base error model, allowing this package to perform as well or better than the widely used Genome Analysis Toolkit (GATK) in all key measures of performance on human whole-genome sequences.

Original languageEnglish (US)
Pages (from-to)E1923-E1932
JournalProceedings of the National Academy of Sciences of the United States of America
Volume114
Issue number10
DOIs
StatePublished - Mar 7 2017
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General

Keywords

  • GATK
  • Genome sequencing
  • SNP calling
  • Sequence mapping
  • Software

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