TRIAGE: A web-based iterative analysis platform integrating pathway and network approaches optimizes hit selection from high- throughput assays.
Samuel Katz, Jian SongiD, Kyle P. Webb, Nicolas LounsburyiD, Clare Elizabeth BryantiD, Iain D. C. FraseriD
Abstract
Comprehensive and efficient gene hit selection from high throughput assays remains a critical bottleneck in realizing the potential of genome-scale studies in biology. Widely used methods such as setting of cutoffs, prioritizing pathway enrichments, or incorporating predicted network interactions offer divergent solutions yet are associated with critical analytical trade-offs, and are often combined in an ad hoc manner. The specific limitations of these individual approaches, the lack of a systematic way by which to integrate their rankings, and the inaccessibility of complex computational approaches to many researchers, has contributed to unexpected variability and limited overlap in the reported results from comparable genome-wide studies. Using a set of three highly studied genome-wide datasets for HIV host factors that have been broadly cited for their limited number of shared candidates, we characterize the specific complementary contributions of commonly used analysis approaches and find an optimal framework by which to integrate these methods. We describe Throughput Ranking by Iterative Analysis of Genomic Enrichment (TRIAGE), an integrated, iterative approach which uses pathway and network statistical methods and publicly available databases to optimize gene prioritization. TRIAGE is accessible as a secure, rapid, user-friendly web-based application (https://triage.niaid.nih.gov). O_FIG O_LINKSMALLFIG WIDTH=197 HEIGHT=200 SRC="FIGDIR/small/204917v2_ufig1.gif" ALT="Figure 1"> View larger version (44K): org.highwire.dtl.DTLVardef@7150f8org.highwire.dtl.DTLVardef@17af411org.highwire.dtl.DTLVardef@12d8f01org.highwire.dtl.DTLVardef@78c48_HPS_FORMAT_FIGEXP M_FIG Graphical Abstract C_FIG
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