9ed6f979a8ec95ac934e5e8fef028d188b76a035 chmalee Mon Aug 6 14:38:57 2018 -0700 pslMismatchGapToBed now outputs a single bed9+ instead of 5 different bed files, refs #21079 diff --git src/hg/lib/txAliDiff.as src/hg/lib/txAliDiff.as new file mode 100644 index 0000000..e5e04b9 --- /dev/null +++ src/hg/lib/txAliDiff.as @@ -0,0 +1,24 @@ +table txAliDiff +"Differences between reference genome and transcript sequences" + ( + string chrom; "Reference sequence chromosome or scaffold" + uint chromStart; "Start position in chromosome of ambiguous gap placement region" + uint chromEnd; "End position in chromosome of ambiguous gap placement region" + string name; "Name of item" + uint score; "Not used" + char[1] strand; "Transcript orientation on genome: + or -" + uint thickStart; "Start position of 3'-most location for gaps that can shift position without introducing mismatches" + uint thickEnd; "End position of 3'-most gap location for gaps that can shift position without introducing mismatches" + uint reserved; "RGB color of this item" + string txName; "Transcript identifier" + uint txStart; "Start position in transcript (of ambiguous gap placement region where applicable)" + uint txEnd; "End position in transcript (of ambiguous gap placement region where applicable)" + uint gSkipped; "Number of bases skipped on genome, if any" + uint txSkipped; "Number of bases skipped on transcript, if any" + uint shiftL; "Number of bases that gap can be shifted left on genome with no mismatches" + uint shiftR; "Number of bases that gap can be shifted right on genome with no mismatches" + lstring hgvsG; "HGVS g. notation of genome change to match transcript" + lstring hgvsCN; "HGVS c./n. notation of part of transcript not matched in genome" + lstring hgvsN; "HGVS c./n. notation of transcript change to match genome" + lstring hgvsPosCN; "HGVS c./n. position range of transcript ambiguous gap placement region" + )