View source: R/POLYFUN_import_priors.R
| POLYFUN_import_priors | R Documentation |
Import SNP-wise prior probabilities pre-computed from many UK Biobank traits.
This function handles finding the intersection of SNPS that exist in the
input GWAS summary stats dat and the pre-computed priors that come
shipped with PolyFun. Then, it saves this subset as a new file for PolyFun
(or other fine-mapping tools) to use as input.
Uses the extract_snpvar.py script from PolyFun.
POLYFUN_import_priors( locus_dir, dat = NULL, polyfun = NULL, force_new_priors = TRUE, remove_tmps = FALSE, nThread = 1, conda_env = "echoR_mini", verbose = TRUE )
https://www.nature.com/articles/s41588-020-00735-5
Other polyfun:
POLYFUN_compute_priors(),
POLYFUN_download_ref_files(),
POLYFUN_find_folder(),
POLYFUN_finemapper(),
POLYFUN_gather_annotations(),
POLYFUN_gather_ldscores(),
POLYFUN_help(),
POLYFUN_initialize(),
POLYFUN_munge_summ_stats(),
POLYFUN_prepare_snp_input(),
POLYFUN_run_ldsc(),
POLYFUN()
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