An example results file after running finemap_loci on the MEX3C locus.

MEX3C

Format

data.table

SNP

SNP RSID

CHR

Chromosome

POS

Genomic positiion (in basepairs)

...

Source

https://www.biorxiv.org/content/10.1101/388165v3

Details

Data originally comes from the Parkinson's disease GWAS by Nalls et al. (bioRxiv).

See also

Other Nalls23andMe_2019: BST1, LRRK2

Examples

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) }