LAUSR

Abstract Combining statistical significances (P‐values) from a set of single‐locus association tests in genome‐wide association studies is a proof‐of‐principle method for identifying disease‐associated genomic segments, functional genes and biological pathways. We review P‐value combinations for genome‐wide association studies and introduce an integrated analysis tool, Omnibus P‐value Association Tests (OPATs), which provides popular analysis methods of P‐value combinations. The software OPATs programmed in R and R graphical user interface features a user‐friendly interface. In addition to analysis modules for data quality control and single‐locus association tests, OPATs provides three types of set‐based association test: window‐, gene‐ and biopathway‐based association tests. P‐value combinations with or without threshold and rank truncation are provided. The significance of a set‐based association test is evaluated by using resampling procedures. Performance of the set‐based association tests in OPATs has been evaluated by simulation studies and real data analyses. These set‐based association tests help boost the statistical power, alleviate the multiple‐testing problem, reduce the impact of genetic heterogeneity, increase the replication efficiency of association tests and facilitate the interpretation of association signals by streamlining the testing procedures and integrating the genetic effects of multiple variants in genomic regions of biological relevance. In summary, P‐value combinations facilitate the identification of marker sets associated with disease susceptibility and uncover missing heritability in association studies, thereby establishing a foundation for the genetic dissection of complex diseases and traits. OPATs provides an easy‐to‐use and statistically powerful analysis tool for P‐value combinations. OPATs, examples, and user guide can be downloaded from http://www.stat.sinica.edu.tw/hsinchou/genetics/association/OPATs.htm.