An example results file after running
finemap_loci
on the BST1 locus.
data("BST1")
data.table
SNP RSID
Chromosome
Genomic position (in basepairs)
Optional: extra columns
data.table
root_dir <- "~/Desktop/Fine_Mapping/Data/GWAS/Nalls23andMe_2019/BST1/Multi-finemap"
BST1 <- data.table::fread(file.path(root_dir, "Multi-finemap_results.txt"))
BST1 <- update_cols(dat = BST1)
BST1 <- find_consensus_SNPs(dat = BST1)
usethis::use_data(BST1, overwrite = TRUE)
Data originally comes from the Parkinson's disease GWAS by Nalls et al., (bioRxiv).