A scalable and portable framework for massively parallel variable selection in genetic association studies

Bioinformatics. 2012 Mar 1;28(5):719-20. doi: 10.1093/bioinformatics/bts015. Epub 2012 Jan 11.

Abstract

The deluge of data emerging from high-throughput sequencing technologies poses large analytical challenges when testing for association to disease. We introduce a scalable framework for variable selection, implemented in C++ and OpenCL, that fits regularized regression across multiple Graphics Processing Units. Open source code and documentation can be found at a Google Code repository under the URL http://bioinformatics.oxfordjournals.org/content/early/2012/01/10/bioinformatics.bts015.abstract.

Supplementary information: Supplementary data are available at Bioinformatics online.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Algorithms*
  • Genome-Wide Association Study*
  • Humans
  • Male
  • Polymorphism, Single Nucleotide
  • Programming Languages
  • Prostatic Neoplasms / ethnology
  • Prostatic Neoplasms / genetics
  • Software*