PheWAS analyze many phenotypes compared to a single genetic variant (or other attribute). This method was originally described using electronic medical record (EMR) data from EMR-linked in the Vanderbilt DNA biobank, BioVU, but can also be applied to other richly phenotyped sets. ::DEVELOPER Biomedical Language Processing Lab
- Linux / Windows/ MacOsX
- R / Perl
:: MORE INFORMATION
Bioinformatics. 2010 May 1;26(9):1205-10. doi: 10.1093/bioinformatics/btq126. Epub 2010 Mar 24.
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Denny JC1, Ritchie MD, Basford MA, Pulley JM, Bastarache L, Brown-Gentry K, Wang D, Masys DR, Roden DM, Crawford DC
Bioinformatics. 2014 May 7.
R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment.
Carroll RJ1, Bastarache L, Denny JC.