An example results file after running
finemap_loci
on the MEX3C locus.
MEX3C
data.table
SNP RSID
Chromosome
Genomic positiion (in basepairs)
https://www.biorxiv.org/content/10.1101/388165v3
Data originally comes from the Parkinson's disease GWAS by Nalls et al. (bioRxiv).
if (FALSE) { root_dir <- "~/Desktop/Fine_Mapping/Data/GWAS/Nalls23andMe_2019" locus_dir <- "MEX3C/Multi-finemap/Multi-finemap_results.txt" MEX3C <- data.table::fread(file.path(root_dir,locus_dir)) MEX3C <- update_CS_cols(finemap_dat=MEX3C) MEX3C <- find_consensus_SNPs(finemap_dat=MEX3C) data.table::fwrite(MEX3C,"inst/extdata/Nalls23andMe_2019/MEX3C_Nalls23andMe_2019_subset.tsv.gz", sep="\t") usethis::use_data(MEX3C, overwrite = T) }