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.
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.
Scripts used for the formatting of files in order to run FINEMAP to calculate causal variant probabilities and downstream analyses
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