Barcelona, España
With the increase in the production of genome-wide association studies (GWAS), the analysis of such data sets with thousands of potential predictive single nucleotide-polymorphisms (SNPs) has become crucial in biomedical research. Here we propose a new method to identify SNPs related with a disease in case-control studies. The method provides two ordered lists of SNPs (with causal or protective alleles) that provide a useful tool to help the researcher to decide where to focus attention in a first stage.
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