a916136b8536d1cea475bd82516fa751726b414b max Wed Jan 24 08:33:49 2024 -0800 adding stars to clinvar, refs #32915 diff --git src/hg/utils/otto/clinvar/clinVarToBed src/hg/utils/otto/clinvar/clinVarToBed index b3dfbf6..fadf2e9 100755 --- src/hg/utils/otto/clinvar/clinVarToBed +++ src/hg/utils/otto/clinvar/clinVarToBed @@ -899,34 +899,35 @@ if len(mouseOverName)>80: mouseOverName = mouseOverName[:80]+"..." #if len(hgvsProt) > 90: #hgvsProt = hgvsProt[:90]+"..." #if len(hgvsCod) > 90: #hgvsCod = hgvsCod[:90]+"..." phenotypeIds, _ = accListToHtml(phenotypeIds) starRatingHtml, asciiStars, starCount = reviewStatusToHtmlStars(reviewStatus) phenotypeList = ", ".join(phenotypeList.split("|")) - mouseOverParts = [mouseOverName, "Type: "+allType, "Consequence: "+ molConseq, "Significance: "+clinSign, + mouseOverParts = [mouseOverName, "Review Status: "+starRatingHtml, + "Type: "+allType, "Consequence: "+ molConseq, "Significance: "+clinSign, "Origin: "+origin, "Phenotypes: "+phenotypeList] # removed Apr 2020: numberSubmitters+" submitters", "Level: "+asciiStars - mouseOver = ", ".join(mouseOverParts) + mouseOver = "<br>".join(mouseOverParts) snpAcc = "rs"+snpAcc # dbSnp links changed in mid/late 2022 row = [chrom, start, end, shortName, str(starCount), strand, thickStart, thickEnd, itemRgb, \ blockCount, blockSizes, blockStarts, name, clinSign, starRatingHtml, allType, geneStr, molConseq, snpAcc, dbVarAcc, irvcAcc, inGtr, phenotypeList, phenotypeIds, origin, assembly, cytogenetic, hgvsTable, "", numberSubmitters, lastEval, guidelines, otherIds, mouseOver, # these fields are the for the filters, not for the display pathoCode, originCode, allTypeCode, str(varLen), str(starCount), # the variant ID got forgotten in the original bigBed schema, it was only part of the origName field varId, dbVarSsvAcc] # replace clinvar's placeholders with real empty fields newRow = []