Sparse group factor analysis for biclustering of multiple data sources

Bioinformatics. 2016 Aug 15;32(16):2457-63. doi: 10.1093/bioinformatics/btw207. Epub 2016 Apr 19.

Abstract

Motivation: Modelling methods that find structure in data are necessary with the current large volumes of genomic data, and there have been various efforts to find subsets of genes exhibiting consistent patterns over subsets of treatments. These biclustering techniques have focused on one data source, often gene expression data. We present a Bayesian approach for joint biclustering of multiple data sources, extending a recent method Group Factor Analysis to have a biclustering interpretation with additional sparsity assumptions. The resulting method enables data-driven detection of linear structure present in parts of the data sources.

Results: Our simulation studies show that the proposed method reliably infers biclusters from heterogeneous data sources. We tested the method on data from the NCI-DREAM drug sensitivity prediction challenge, resulting in an excellent prediction accuracy. Moreover, the predictions are based on several biclusters which provide insight into the data sources, in this case on gene expression, DNA methylation, protein abundance, exome sequence, functional connectivity fingerprints and drug sensitivity.

Availability and implementation: http://research.cs.aalto.fi/pml/software/GFAsparse/

Contacts: : kerstin.bunte@googlemail.com or samuel.kaski@aalto.fi.

MeSH terms

  • Algorithms*
  • Bayes Theorem
  • Cluster Analysis*
  • Datasets as Topic*
  • Factor Analysis, Statistical
  • Gene Expression Profiling*
  • Information Storage and Retrieval
  • Oligonucleotide Array Sequence Analysis