# HG changeset patch
# User iuc
# Date 1658583486 0
# Node ID 8627b2b383b4bf78aab1dfceac52230a78ac700e
# Parent  8d637025a9057ec7b6cf39fc42764470c44896fe
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bcftools commit c45135e52ae5039e09272ac6f504d0ceb574aa70

diff -r 8d637025a905 -r 8627b2b383b4 test-data/plugin2.vcf
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/plugin2.vcf	Sat Jul 23 13:38:06 2022 +0000
@@ -0,0 +1,13 @@
+##fileformat=VCFv4.2
+##FILTER=<ID=PASS,Description="All filters passed">
+##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype code">
+##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype quality">
+##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read depth">
+##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Read depth for each allele">
+##FORMAT=<ID=ADF,Number=R,Type=Integer,Description="Read depth for each allele on the forward strand">
+##FORMAT=<ID=ADR,Number=R,Type=Integer,Description="Read depth for each allele on the reverse strand">
+##INFO=<ID=ANN,Number=.,Type=String,Description="Consequence annotations from Ensembl VEP. Format: Allele|Consequence|IMPACT|SYMBOL|Gene|Feature_type|Feature|BIOTYPE|EXON|INTRON|HGVSc|HGVSp|cDNA_position|CDS_position|Protein_position|Amino_acids|Codons|Existing_variation|DISTANCE|STRAND|FLAGS|SYMBOL_SOURCE|HGNC_ID|SIFT|PolyPhen|gnomAD_AF|gnomAD_AFR_AF|gnomAD_AMR_AF|gnomAD_ASJ_AF|gnomAD_EAS_AF|gnomAD_FIN_AF|gnomAD_NFE_AF|gnomAD_OTH_AF|gnomAD_SAS_AF|CLIN_SIG|SOMATIC|PHENO|CAROL|Condel">
+#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	NORMAL	TUMOR
+chr12	247923	.	A	G	.	PASS	ANN=G|missense_variant|MODERATE|IQSEC3|ENSG00000120645|Transcript|ENST00000326261|protein_coding|4/15||||1394|1394|465|D/G|gAt/gGt|rs75677829||1||HGNC|29193|tolerated(0.23)|benign(0.015)|0.08|0.2314|0.05139|0.1233|0.01977|0.09129|0.08025|0.07976|0.07557||||Neutral(0.763)|neutral(0.042),G|missense_variant|MODERATE|IQSEC3|ENSG00000120645|Transcript|ENST00000382841|protein_coding|3/13||||897|485|162|D/G|gAt/gGt|rs75677829||1||HGNC|29193|tolerated_low_confidence(0.32)|benign(0.036)|0.08|0.2314|0.05139|0.1233|0.01977|0.09129|0.08025|0.07976|0.07557||||Neutral(0.659)|neutral(0.026),G|intron_variant&non_coding_transcript_variant|MODIFIER|RP11-598F7.4|ENSG00000249695|Transcript|ENST00000505893|antisense||7/9||||||||rs75677829||-1||Clone_based_vega_gene||||0.08|0.2314|0.05139|0.1233|0.01977|0.09129|0.08025|0.07976|0.07557|||||,G|downstream_gene_variant|MODIFIER|RP11-598F7.4|ENSG00000249695|Transcript|ENST00000508953|antisense||||||||||rs75677829|777|-1||Clone_based_vega_gene||||0.08|0.2314|0.05139|0.1233|0.01977|0.09129|0.08025|0.07976|0.07557|||||,G|missense_variant|MODERATE|IQSEC3|ENSG00000120645|Transcript|ENST00000538872|protein_coding|4/14||||1512|1394|465|D/G|gAt/gGt|rs75677829||1||HGNC|29193|tolerated(0.23)|benign(0.015)|0.08|0.2314|0.05139|0.1233|0.01977|0.09129|0.08025|0.07976|0.07557||||Neutral(0.763)|neutral(0.042)	GT:GQ:DP:AD:ADF:ADR	0/1:.:14:8,6:7,6:1,0	0/1:.:41:12,29:10,25:2,4
+chr12	284058	.	T	C	.	PASS	ANN=C|synonymous_variant|LOW|IQSEC3|ENSG00000120645|Transcript|ENST00000326261|protein_coding|14/15||||3408|3408|1136|G|ggT/ggC|rs216230&COSV58289061||1||HGNC|29193|||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|downstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000382841|protein_coding||||||||||rs216230&COSV58289061|3562|1||HGNC|29193|||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|non_coding_transcript_exon_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000537151|processed_transcript|3/4||||378|||||rs216230&COSV58289061||1||HGNC|29193|||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|intron_variant&non_coding_transcript_variant|MODIFIER|RP11-598F7.6|ENSG00000256540|Transcript|ENST00000537295|lincRNA||1/2||||||||rs216230&COSV58289061||-1||Clone_based_vega_gene||||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|intron_variant&non_coding_transcript_variant|MODIFIER|RP11-598F7.6|ENSG00000256540|Transcript|ENST00000537961|lincRNA||1/1||||||||rs216230&COSV58289061||-1||Clone_based_vega_gene||||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|synonymous_variant|LOW|IQSEC3|ENSG00000120645|Transcript|ENST00000538872|protein_coding|14/14||||3526|3408|1136|G|ggT/ggC|rs216230&COSV58289061||1||HGNC|29193|||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|downstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000540907|retained_intron||||||||||rs216230&COSV58289061|3426|1||HGNC|29193|||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||,C|upstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000544511|processed_transcript||||||||||rs216230&COSV58289061|1590|1||HGNC|29193|||0.9443|0.9477|0.967|0.9298|0.8657|0.944|0.9597|0.9377|0.9158||0&1|0&1||	GT:GQ:DP:AD:ADF:ADR	1/1:.:13:0,13:0,5:0,8	1/1:.:48:0,48:0,14:0,34
+chr12	285027	.	C	A	.	PASS	ANN=A|3_prime_UTR_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000326261|protein_coding|14/15||||4377|||||rs7960096||1||HGNC|29193||||||||||||||||,A|downstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000382841|protein_coding||||||||||rs7960096|4531|1||HGNC|29193||||||||||||||||,A|downstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000537151|processed_transcript||||||||||rs7960096|502|1||HGNC|29193||||||||||||||||,A|intron_variant&non_coding_transcript_variant|MODIFIER|RP11-598F7.6|ENSG00000256540|Transcript|ENST00000537295|lincRNA||1/2||||||||rs7960096||-1||Clone_based_vega_gene|||||||||||||||||,A|intron_variant&non_coding_transcript_variant|MODIFIER|RP11-598F7.6|ENSG00000256540|Transcript|ENST00000537961|lincRNA||1/1||||||||rs7960096||-1||Clone_based_vega_gene|||||||||||||||||,A|3_prime_UTR_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000538872|protein_coding|14/14||||4495|||||rs7960096||1||HGNC|29193||||||||||||||||,A|downstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000540907|retained_intron||||||||||rs7960096|4395|1||HGNC|29193||||||||||||||||,A|upstream_gene_variant|MODIFIER|IQSEC3|ENSG00000120645|Transcript|ENST00000544511|processed_transcript||||||||||rs7960096|621|1||HGNC|29193||||||||||||||||	GT:GQ:DP:AD:ADF:ADR	0/1:.:25:15,10:10,7:5,3	0/1:.:19:8,11:3,8:5,3