| xQTLanalyze_coloc_diy | R Documentation | 
Conduct colocalization analysis with customized QTL data
xQTLanalyze_coloc_diy(
  gwasDF,
  qtlDF,
  mafThreshold = 0.01,
  gwasSampleNum = 50000,
  qtlSampleNum = 10000,
  method = "coloc",
  bb.alg = FALSE
)
| gwasDF | data.frame or data.table, required cols: rsid, chrom, position, pValue, maf, beta, se | 
| qtlDF | data.frame or data.table, required cols: rsid, chrom, position, pValue, maf, beta, se | 
| mafThreshold | Cutoff of maf to remove rare variants. | 
| gwasSampleNum | Sample number of GWAS dataset. Default:50000. | 
| qtlSampleNum | Sample number of QTL dataset. Default:10000. | 
| method | (character) options: "coloc"(default) or "hyprcoloc" (need a highe version). | 
| bb.alg | For  | 
A list
url1 <- "http://bioinfo.szbl.ac.cn/xQTL_biolinks/xqtl_data/gwasDFsub_MMP7.txt"
url2 <- "http://bioinfo.szbl.ac.cn/xQTL_biolinks/xqtl_data/eqtl/MMP7_qtlDF.txt"
gwasDF <- data.table::fread(url1)
qtlDF <- data.table::fread(url2)
output <- xQTLanalyze_coloc_diy(gwasDF = gwasDF, qtlDF=qtlDF, method="coloc")
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