A flexible tool for the multi-resolution localization of causal variants across the genome, accounting for population structure.
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Updated
Jul 7, 2022 - C++
A flexible tool for the multi-resolution localization of causal variants across the genome, accounting for population structure.
Scripts used for the formatting of files in order to run FINEMAP to calculate causal variant probabilities and downstream analyses
This method incorporates dense linkage disequilibrium block structure of SNPs for prioritizing a set of genetic variants using GWAS summary statisticis before performing fine-mapping.
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