bioRxivGeneticsPreprint
FORGE: multivariate calculation of gene-wide p-values from Genome-Wide Association Studies Authors and Affiliations
Inti Inal PedrosoiD, Michael R Barnes, Anbarasu Lourdusamy, Ammar Al-Chalabi, Gerome Breen
Abstract
Genome-wide association studies (GWAS) have proven a valuable tool to explore the genetic basis of many traits. However, many GWAS lack statistical power and the commonly used single-point analysis method needs to be complemented to enhance power and interpretation. Multivariate region or gene-wide association are an alternative, allowing for identification of disease genes in a manner more robust to allelic heterogeneity. Gene-based association also facilitates systems biology analyses by generating a single p-value per gene. We have designed and implemented FORGE, a software suite which implements a range of methods for the combination of p-values for the individual genetic variants within a gene or genomic region. The software can be used with summary statistics (marker ids and p-values) and accepts as input the result file formats of commonly used genetic association software. When applied to a study of Crohns disease susceptibility, it identified all genes found by single SNP analysis and additional genes identified by large independent metaanalysis. FORGE p-values on gene-set analyses highlighted association with the Jak-STAT and cytokine signalling pathways, both previously associated with CD. We highlight the softwares main features, its future development directions and provide a comparison with alternative available software tools. FORGE can be freely accessed at https://github.com/inti/FORGE.
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- research focus: benchmarking
- research focus: software / tool
- approach: statistical model
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