Each folder here has the following format:
<run_order_number>_<description_of_what_is_done>
/
Each folder has the following subfolders, each with their own README.md:
code/
input/
output/
Please see the individual subfolder README.md files for further information.
00_prep_inputs_for_metaxcan/
- This folder prepares raw GWAS information for MetaXcan's SPrediXcan process.
- This includes METAL, GWAS parsing, and summary imputation to variants used in predictdb.org's GTEX V8 mashr models.
010_ukb_bcac_meta_new_loci/
- This folder contains a GWAS analysis of the meta-analysis of UKB/BCAC for overall breast cancer to find newly identified GWAS variants.
01_spredixcan_eqtl_sqtl/
- This folder contains the SPrediXcan related code/input/output.
02_acat_eqtl_sqtl
- Contains the ACAT (p-value combination method) results.
03_enloc/
- Finemapping enloc.
04_cojo_ctwas/
- Contains conditional joint analysis (COJO) and the subsequent conditional TWAS (CTWAS) based on the COJO results.
- Due to computational strain only Bonferroni significant variants from each study are run through the COJO/CTWAS process.
05_focus:
- Contains Bogdan Lab's FOCUS resuls for our studies of interest.
08_expression_pred_ccv:
- Contains code/input/output pertaining to the enrichment of credible causal variant (CCVs), made recently to address AJHG reviewer comments.
999_reporting_friendly_tables:
- Contains precursor tables to those final tables presented in the paper. Convenient files for genetic distances, gencode 26 to 40 conversion, are included.