Repository 'bbtools_bbmap'
hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/bbtools_bbmap

Changeset 1:17ad142b56e6 (2021-10-05)
Previous changeset 0:07a6e49c7d74 (2021-10-04) Next changeset 2:e0ca2ec4f5d9 (2021-11-11)
Commit message:
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bbtools commit 56300a95740ee11e84a7d0bda07a71fbaf4952e4"
added:
test-data/cv_input.bam
test-data/cv_output.gff
test-data/cv_output.txt
test-data/cv_output.vcf
test-data/cv_qualityhist_output.tabular
test-data/cv_scorehist_output.tabular
test-data/cv_zygosityhist_output.tabular
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_input.bam
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Binary file test-data/cv_input.bam has changed
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_output.gff
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cv_output.gff Tue Oct 05 20:06:15 2021 +0000
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@@ -0,0 +1,18 @@
+##gff-version
+#BBMapVersion
+#ploidy 2
+#rarity 1.00000
+#minAlleleFraction 0.1000
+#reads 2207
+#pairedReads 0
+#properlyPairedReads 0
+#readLengthAvg
+#properPairRate 0.0000
+#totalQualityAvg
+#mapqAvg
+#reference
+#seqid source type start end score strand phase attributes
+NC_002945.4 . sequence_variant_obs 976327 976327
+NC_002945.4 . sequence_variant_obs 1501932 1501932
+NC_002945.4 . sequence_variant_obs 3380579 3380579
+NC_002945.4 . sequence_variant_obs 3646293 3646293
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_output.txt
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cv_output.txt Tue Oct 05 20:06:15 2021 +0000
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@@ -0,0 +1,18 @@
+#fileformat
+#BBMapVersion
+#ploidy 2
+#rarity 1.00000
+#minAlleleFraction 0.1000
+#reads 2207
+#pairedReads 0
+#properlyPairedReads 0
+#readLengthAvg
+#properPairRate
+#totalQualityAvg
+#mapqAvg
+#reference
+#scaf start stop type call r1p r1m r2p r2m paired lengthSum mapq mapqMax baseq baseqMax edist edistMax id idMax cov minusCov nearbyVarCount flagged contigEndDist phredScore readCount alleleFraction revisedAF strandRatio baseqAvg mapqAvg edistAvg identityAvg edistScore identityScore qualityScore pairedScore biasScore coverageScore homopolymerScore score
+0 976326 976327 SUB T
+0 1501931 1501932 SUB C
+0 3380578 3380579 SUB G
+0 3646292 3646293 SUB A
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_output.vcf
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cv_output.vcf Tue Oct 05 20:06:15 2021 +0000
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@@ -0,0 +1,60 @@
+##fileformat=VCFv4.2
+##BBMapVersion=
+##ploidy=2
+##rarity=1.00000
+##minallelefraction=0.10000
+##reads=2207
+##pairedReads=0
+##properlyPairedReads=0
+##readLengthAvg=
+##properPairRate=0.00000
+##totalQualityAvg=
+##mapqAvg=43.348
+##reference=
+##contig=<ID=NC_002945.4,length=7000>
+##FILTER=<ID=FAIL,Description="Fail">
+##FILTER=<ID=PASS,Description="Pass">
+##INFO=<ID=SN,Number=1,Type=Integer,Description="Scaffold Number">
+##INFO=<ID=STA,Number=1,Type=Integer,Description="Start">
+##INFO=<ID=STO,Number=1,Type=Integer,Description="Stop">
+##INFO=<ID=TYP,Number=1,Type=String,Description="Type">
+##INFO=<ID=R1P,Number=1,Type=Integer,Description="Read1 Plus Count">
+##INFO=<ID=R1M,Number=1,Type=Integer,Description="Read1 Minus Count">
+##INFO=<ID=R2P,Number=1,Type=Integer,Description="Read2 Plus Count">
+##INFO=<ID=R2M,Number=1,Type=Integer,Description="Read2 Minus Count">
+##INFO=<ID=AD,Number=1,Type=Integer,Description="Allele Depth">
+##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
+##INFO=<ID=MCOV,Number=1,Type=Integer,Description="Minus Coverage">
+##INFO=<ID=PPC,Number=1,Type=Integer,Description="Paired Count">
+##INFO=<ID=AF,Number=1,Type=Float,Description="Allele Fraction">
+##INFO=<ID=RAF,Number=1,Type=Float,Description="Revised Allele Fraction">
+##INFO=<ID=LS,Number=1,Type=Integer,Description="Length Sum">
+##INFO=<ID=MQS,Number=1,Type=Integer,Description="MAPQ Sum">
+##INFO=<ID=MQM,Number=1,Type=Integer,Description="MAPQ Max">
+##INFO=<ID=BQS,Number=1,Type=Integer,Description="Base Quality Sum">
+##INFO=<ID=BQM,Number=1,Type=Integer,Description="Base Quality Max">
+##INFO=<ID=EDS,Number=1,Type=Integer,Description="End Distance Sum">
+##INFO=<ID=EDM,Number=1,Type=Integer,Description="End Distance Max">
+##INFO=<ID=IDS,Number=1,Type=Integer,Description="Identity Sum">
+##INFO=<ID=IDM,Number=1,Type=Integer,Description="Identity Max">
+##INFO=<ID=NVC,Number=1,Type=Integer,Description="Nearby Variation Count">
+##INFO=<ID=FLG,Number=1,Type=Integer,Description="Flagged">
+##INFO=<ID=CED,Number=1,Type=Integer,Description="Contig End Distance">
+##INFO=<ID=HMP,Number=1,Type=Integer,Description="Homopolymer Count">
+##INFO=<ID=SB,Number=1,Type=Float,Description="Strand Bias">
+##INFO=<ID=DP4,Number=4,Type=Integer,Description="Ref+, Ref-, Alt+, Alt-">
+##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
+##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
+##FORMAT=<ID=AD,Number=1,Type=Integer,Description="Allele Depth">
+##FORMAT=<ID=AF,Number=1,Type=Float,Description="Allele Fraction">
+##FORMAT=<ID=RAF,Number=1,Type=Float,Description="Revised Allele Fraction">
+##FORMAT=<ID=NVC,Number=1,Type=Integer,Description="Nearby Variation Count">
+##FORMAT=<ID=FLG,Number=1,Type=Integer,Description="Flagged">
+##FORMAT=<ID=SB,Number=1,Type=Float,Description="Strand Bias">
+##FORMAT=<ID=SC,Number=1,Type=Float,Description="Score">
+##FORMAT=<ID=PF,Number=1,Type=String,Description="Pass Filter">
+#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT
+NC_002945.4 976327 . N T 22.21 PASS SN=0;STA=976326;STO=976327;TYP=SUB;R1P=2;R1M=0;R2P=0;R2M=0;AD=2;DP=2;MCOV=-1;PPC=0;AF=1.0000;RAF=1.0000;LS=292;MQS=77;MQM=40;BQS=48;BQM=24;EDS=111;EDM=65;IDS=1930;IDM=972;NVC=0;FLG=0;CED=0;HMP=0;SB=0.9980 GT:DP:AD:AF:RAF:NVC:FLG:SB:SC:PF 1/1:2:2:1.0000:1.0000:0:0:0.9980:22.21:PASS
+NC_002945.4 1501932 . N C 27.20 PASS SN=0;STA=1501931;STO=1501932;TYP=SUB;R1P=0;R1M=2;R2P=0;R2M=0;AD=2;DP=2;MCOV=-1;PPC=0;AF=1.0000;RAF=1.0000;LS=292;MQS=88;MQM=44;BQS=64;BQM=39;EDS=74;EDM=38;IDS=1986;IDM=993;NVC=0;FLG=0;CED=0;HMP=0;SB=0.9980 GT:DP:AD:AF:RAF:NVC:FLG:SB:SC:PF 1/1:2:2:1.0000:1.0000:0:0:0.9980:27.20:PASS
+NC_002945.4 3380579 . N G 27.85 PASS SN=0;STA=3380578;STO=3380579;TYP=SUB;R1P=0;R1M=2;R2P=0;R2M=0;AD=2;DP=2;MCOV=-1;PPC=0;AF=1.0000;RAF=1.0000;LS=289;MQS=87;MQM=44;BQS=75;BQM=38;EDS=105;EDM=63;IDS=1986;IDM=993;NVC=0;FLG=0;CED=0;HMP=0;SB=0.9980 GT:DP:AD:AF:RAF:NVC:FLG:SB:SC:PF 1/1:2:2:1.0000:1.0000:0:0:0.9980:27.85:PASS
+NC_002945.4 3646293 . N A 23.34 PASS SN=0;STA=3646292;STO=3646293;TYP=SUB;R1P=1;R1M=1;R2P=0;R2M=0;AD=2;DP=2;MCOV=-1;PPC=0;AF=1.0000;RAF=1.0000;LS=291;MQS=86;MQM=44;BQS=76;BQM=38;EDS=44;EDM=31;IDS=1986;IDM=993;NVC=0;FLG=0;CED=0;HMP=0;SB=1.0000 GT:DP:AD:AF:RAF:NVC:FLG:SB:SC:PF 1/1:2:2:1.0000:1.0000:0:0:1.0000:23.34:PASS
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_qualityhist_output.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cv_qualityhist_output.tabular Tue Oct 05 20:06:15 2021 +0000
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@@ -0,0 +1,46 @@
+#BaseQualityHist
+#Vars
+#Mean
+#Median
+#Mode
+#Quality AvgCount MaxCount
+0 0 0
+1 0 0
+2 0 0
+3 0 0
+4 0 0
+5 0 0
+6 0 0
+7 0 0
+8 0 0
+9 0 0
+10 0 0
+11 0 0
+12 0 0
+13 0 0
+14 0 0
+15 0 0
+16 0 0
+17 0 0
+18 0 0
+19 0 0
+20 0 0
+21 0 0
+22 0 0
+23 0 0
+24 1 1
+25 0 0
+26 0 0
+27 0 0
+28 0 0
+29 0 0
+30 0 0
+31 0 0
+32 1 0
+33 0 0
+34 0 0
+35 0 0
+36 0 0
+37 1 0
+38 1 2
+39 0 1
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_scorehist_output.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cv_scorehist_output.tabular Tue Oct 05 20:06:15 2021 +0000
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@@ -0,0 +1,34 @@
+#ScoreHist
+#Vars
+#Mean
+#Median
+#Mode
+#Quality Count
+0 0
+1 0
+2 0
+3 0
+4 0
+5 0
+6 0
+7 0
+8 0
+9 0
+10 0
+11 0
+12 0
+13 0
+14 0
+15 0
+16 0
+17 0
+18 0
+19 0
+20 0
+21 0
+22 1
+23 1
+24 0
+25 0
+26 0
+27 2
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diff -r 07a6e49c7d74 -r 17ad142b56e6 test-data/cv_zygosityhist_output.tabular
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/cv_zygosityhist_output.tabular Tue Oct 05 20:06:15 2021 +0000
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@@ -0,0 +1,8 @@
+#ZygoHist
+#Vars
+#Mean
+#HomozygousFraction
+#Zygosity Count
+0 0
+1 0
+2 4