To understand the funtion of Colorectal cancer GWAS results, we perform a comprehensive analysis using biofeatures of HCT116 colon cancer cell line and got a list of risk-asscociated SNP. Risk-associa
Pre-computed lists of ‘variant pairs’ with one ClinVar variant and one variant not in ClinVar (any possible nsSNV from dbNSFP) for - PS1 Strong Evidence (Unclassified and P/LP variant encoding the sam
This dataset is from the paper "Extracting and calibrating evidence of variant pathogenicity from population biobank data", which evaluates the broad potential of using population cohort data as evide
Experimental set accompanying Giacomini et al publication "A legacy gene-expression signature of genetic instability in colon cancer". Includes 18 colon cancer cell line training set, 13 colon cancer
Interventions: The aim of this research is to find the undiscovered gene or genes responsible for hereditary colorectal cancer, and to understand how the gene(s) cause colorectal cancer. One of the be