This page contains all command available in BridgePRS.
Tips
When constructing new parameters, we follow the following rule: if the command has effect on any file that is not the target,
it will have a prefix of the file name. For example, --base-info applies INFO score filtering on the base file, --ld-info perform INFO score filtering on the LD reference file and --info applies the INFO score filtering on the target file.
Input Population Files/Arguments
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--sumstats_prefixPath to sumstats data -
--sumstats_suffixSumstats Suffix -
--phenotype_filesphenotype test and validation data -
--pop_config(s)population configuration file(s) -
--pop or --popspopulation names (AFR, EUR, etc) -
--snp_fileList of QCed SNP ids
System Level Toggles/Arguments
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--coresBy default bridgePRS is parralelized across (n-1) cores -
-oOutput folder for BridgePRS -
--platformForce platform (Linux or MacOS) -
--verboseToggle Verbose Mode On -
--noPlotsSkip Post-Pipeline Analysis (Plotting) -
--restartRepeat previously completed steps
Parameter Arguments
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--fstfst between populations analysed, e.g. 0.15 for Africans v Europeans and 0.11 for East Asians v Europeans -
--strand_checkLogical to check whether summary statistics and reference data input files are on the same strand. If true/1 only unambiguous SNPs are used in analyses. If false/0 all variants with matching alleles between studies are used. With both options effect and reference alleles are checked and flipped where necessary. If a matching pair of alleles is not found variants are removed (default 0) -
--max_clump_sizeMaximum number SNPs allowed in a clump. Very large clumps, eg more than 1,000 variants, can occur in regions of high LD such as the HLA region when using imputed data and considerably slow the algorithm. Must be used in conjunction with--thinned_snplist, see below -
--thinned_snplistThinned snp list to use for clumps that exceed--max_clump_size, list of HapMap variants would be suitable
Internal File Arguments
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--model_filemodel result generated from the build-model subprogram -
--clump_prefixprefix for files generated by clump step -
--beta_prefixprefix for files generated by beta step -
--predict_prefixprefix for files generated by predict step -
--result_fileprs result files
File Column Names
Phenotype Files
--phenotypePhenotype File Field: phenotype--covariatesPhenotype File Field: comma separated list of covariates
Sumstats Files
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--ssf-snpidSumstats field: snp ID -
--ssf-refSumstats Field: reference allele -
--ssf-altSumstats Field: alt allele -
--ssf-mafSumstats Field: MAF -
--ssf-betaSumstats Field: linear regression effect or log odds -
--ssf-seSumstats field: standard error -
--ssf-pSumstats field: P-value -
--ssf-nSumstats Field: Sample Size