Using graded response model for the prediction of prostate cancer risk.
Ontology highlight
ABSTRACT: Disease risk-associated single nucleotide polymorphisms (SNPs) identified from genome-wide association studies (GWAS) have the potential to be used for disease risk prediction. An important feature of these risk-associated SNPs is their weak individual effect but stronger cumulative effect on disease risk. To date, a stable summary estimate of the joint effect of genetic variants on disease risk prediction is not available. In this study, we propose to use the graded response model (GRM), which is based on the item response theory, for estimating the individual risk that is associated with a set of SNPs. We compare the GRM with a recently proposed risk prediction model called cumulative relative risk (CRR). Thirty-three prostate cancer risk-associated SNPs were originally discovered in GWA
SUBMITTER: Chen SH
PROVIDER: S-EPMC3734950 | biostudies-literature | 2012 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA