Prioritizes genes for disease association. fitSNPs provides a list of functionally interpolating single nucleotide polymorphisms (SNPs) from differential gene expression. It can be loaded into the University of California Santa Cruz (UCSC) genome graph and visualized on the human genome along with a wealth of preloaded or user-defined genomic data, such as genome-wide association studies (GWASs) results.
Stanford Center for Biomedical Informatics Research, Stanford, CA, USA; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA; Lucile Packard Children's Hospital, Palo Alto, CA, USA; NuMedii Inc., CA, USA
fitSNPs funding source(s)
Supported by Lucile Packard Foundation for Children's Health, US National Library of Medicine (K22 LM008261), National Institute of General Medical Sciences (R01 GM079719), Howard Hughes Medical Institute, and Pharmaceutical Research and Manufacturers of America Foundation.