BioinformaticsBioinformaticsPeer-reviewed journal article
bcGST - an interactive bias-correction method to identify over-represented gene-sets in boutique arrays
Kevin Y. X. WangiD, Alexander Maxwell MenziesiD, Inês Pires da SilvaiD, James S. WilmottiD, Yibing Yan, Matthew J. WongchenkoiD, Richard F. KeffordiD, Richard A. ScolyeriD, Georgina Venetia LongiD, Garth TarriD, Samuel Mueller, Jean Yee Hwa YangiD
Abstract
Motivation: Gene annotation and pathway databases such as Gene Ontology and Kyoto Encyclopedia of Genes and Genomes are important tools in Gene Set Test (GST) that describe gene biological functions and associated pathways. GST aims to establish an association relationship between a gene set of interest and an annotation. Importantly, GST tests for over-representation of genes in an annotation term. One implicit assumption of GST is that the gene expression platform captures the complete or a very large proportion of the genome. However, this assumption is neither satisfied for the increasingly popular boutique array nor the custom designed gene expression profiling platform. Specifically, conventional GST is no longer appropriate due to the gene set selection bias induced during the construction of these platforms.\n\nResults: We propose bcGST, a bias-corrected Gene Set Test by introducing bias correction terms in the contingency table needed for calculating the Fishers Exact Test (FET). The adjustment method works by estimating the proportion of genes captured on the array with respect to the genome in order to assist filtration of annotation terms that would otherwise be falsely included or excluded. We illustrate the practicality of bcGST and its stability through multiple differential gene expression analyses in melanoma and TCGA cancer studies.\n\nAvailability: The bcGST method is made available as a Shiny web application at http://shiny.maths.usyd.edu.au/bcGST/\n\nContact: kevin.wang@sydney.edu.au
- Citations
- 1
- FWCI
- 0.09
- Field percentile
- 43th percentile
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