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b/man/shaPRS_LDGen.Rd |
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% Generated by roxygen2: do not edit by hand |
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% Please edit documentation in R/shaPRS.R |
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\name{shaPRS_LDGen} |
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\alias{shaPRS_LDGen} |
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\title{Convenience function to generate a shaPRS specific LD reference panel for cross-ancestry analyses} |
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\usage{ |
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shaPRS_LDGen( |
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Pop1LDRefLoc, |
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Pop2LDRefLoc, |
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blendFactorLoc, |
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adjustinputLoc, |
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outputLoc, |
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discardAmbiguousSNPs = F, |
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memoryEfficiency = 5 |
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) |
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} |
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\arguments{ |
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\item{Pop1LDRefLoc}{Location of the folder of the LDpred2 formatted LD-reference matrices for the 22 autosomes together with a map.rds file for the proximal study} |
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\item{Pop2LDRefLoc}{Location of the folder of the LDpred2 formatted LD-reference matrices for the 22 autosomes together with a map.rds file for the adjunct study} |
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\item{blendFactorLoc}{Location for the lFDR data file produced by shaPRS(), postfix: "_SNP_lFDR"} |
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\item{adjustinputLoc}{Location for the file produced by the shaPRS(), postfix: "_adjustinput"} |
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\item{outputLoc}{Output location} |
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\item{discardAmbiguousSNPs}{(optional) if ambiguous SNPs (G/C and A/T) should be discarded (default TRUE)} |
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\item{memoryEfficiency}{(optional) larger numbers result in longer runs but lower memory usage (default 5)} |
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} |
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\description{ |
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Wrapper function that loads and processes the LD data for two populations, aligns it with summary data for shaPRS and then generate a full new LD-ref panel for 22 autosomes (this should be used instead of LDRefBlend) |
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} |
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\examples{ |
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Pop1LDRefLoc <- paste0(system.file("extdata", "", package = "shaPRS"), "/") |
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Pop2LDRefLoc <- paste0(system.file("extdata", "", package = "shaPRS"), "/") |
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blendFactorLoc <- system.file("extdata", "pop_SNP_lFDR", package = "shaPRS") |
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adjustinputLoc <- system.file("extdata", "pop_adjustinput", package = "shaPRS") |
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outputLoc <- "<YOUR LOCATION>" |
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# shaPRS_LDGen(Pop1LDRefLoc, Pop2LDRefLoc, blendFactorLoc, adjustinputLoc, outputLoc) |
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} |