Click on a button corresponding to a genetic marker process. Refer to the table below for guidance.
Exploring several properties of all markers in a data set, in detail, for quality control (QC) and/or selecting markers to be removed from the analysis Testing for significant differences in missing genotype proportions between cases and controls (or any two groups) for each individual marker Creating blocks of consecutive SNPs based on those in strong linkage disequilibrium (LD) according to specified thresholds Calculating various measurements of, and conducting an overall test for, linkage disequilibrium, between pairs of markers Using a binning algorithm to separate SNPs into bins, and identifying tagSNPs that can be used to represent all SNPs in a bin Describing and summarizing variations in patterns of linkage disequilibrium (LD) across large DNA regions