BioinformaticsBioinformaticsPeer-reviewed journal article
PatternMarkers & GWCoGAPS for novel data-driven biomarkers via whole transcriptome NMF
Genevieve Stein-O’BrieniD, Jacob CareyiD, Wai Shing Lee, Michael ConsidineiD, Alexander V. FavoroviD, Emily L. FlamiD, Theresa W. GuoiD, Sijia LiiD, Luigi MarchionniiD, Thomas D. Sherman, Shawn Sivy, Daria A. GaykalovaiD, Ronald D.G. McKay, Michael F. Ochs, Carlo ColantuoniiD, Elana Judith FertigiD
Abstract
SummaryNon-negative Matrix Factorization (NMF) algorithms associate gene expression with biological processes (e.g., time-course dynamics or disease subtypes). Compared with univariate associations, the relative weights of NMF solutions can obscure biomarkers. Therefore, we developed a novel PatternMarkers statistic to extract genes for biological validation and enhanced visualization of NMF results. Finding novel and unbiased gene markers with PatternMarkers requires whole-genome data. However, NMF algorithms typically do not converge for the tens of thousands of genes in genome-wide profiling. Therefore, we also developed Genome-Wide CoGAPS Analysis in Parallel Sets (GWCoGAPS), the first robust whole genome Bayesian NMF using the sparse, MCMC algorithm, CoGAPS. This software contains analytic and visualization tools including a Shiny web application, patternMatcher, which are generalized for any NMF. Using these tools, we find granular brain-region and cell-type specific signatures with corresponding biomarkers in GTex data, illustrating GWCoGAPS and patternMarkers ascertainment of data-driven biomarkers from whole-genome data.\n\nAvailabilityPatternMarkers & GWCoGAPS are in the CoGAPS Bioconductor package (3.5) under the GPL license.\n\nContactgsteinobrien@jhmi.edu; ccolantu@jhmi.edu; ejfertig@jhmi.edu
- organism: human
- assay: whole-genome sequencing
- research focus: differential expression
- approach: statistical model
- Citations
- 54
- FWCI
- 2.35
- Field percentile
- top 11%
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