Matches automatically phenotype to genes from a defined genome region or a group of given genes. PGMapper combines the mapping information from the Ensembl database and gene function information from the OMIM and PubMed databases. It can be used in whole genome analysis of a complex trait or disease and is able to identify the candidate genes of a quantitative trait loci (QTL) or a disease locus.
Department of Orthopedic Surgery-Campbell Clinic, University of Tennessee Health Science Center, Memphis, TN, USA; Department of Computer Science and Technology, Southwest University, Chongqing, China
PGMapper funding source(s)
Supported by the Center of Excellence for Genomics and Bioinformatics at the University of Tennessee Health Science Center and by the NIH, National Institute of Arthritis and Musculoskeletal and Skin Diseases, AR51190.