Miscellaneous |
Version lineage of this tool (guids ordered most recent to oldest) |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.15.1+galaxy1 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.15.1+galaxy0 (this tool) |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.10 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.9+galaxy1 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.9 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.4.0 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.3.2.0 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.3.2 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.3.0 |
toolshed.g2.bx.psu.edu/repos/iuc/bcftools_call/bcftools_call/1.2.0 |
bcftools_call |
Requirements (dependencies defined in the <requirements> tag set) |
name | version | type |
bcftools | 1.15.1 | package |
htslib | 1.15.1 | package |
Additional information about this tool |
export BCFTOOLS_PLUGINS=`which bcftools | sed 's,bin/bcftools,libexec/bcftools,'`; ## May need to symlink input if there is an associated #set $input_vcf = 'input.vcf.gz' #if $input_file.is_of_type('vcf') bgzip -c '$input_file' > $input_vcf && bcftools index $input_vcf && ##elif $input_file.is_of_type('vcf_bgzip') or $input_file.is_of_type('vcf.gz') #elif $input_file.is_of_type('vcf_bgzip') ln -s '$input_file' $input_vcf && #if $input_file.metadata.tabix_index: ln -s '${input_file.metadata.tabix_index}' ${input_vcf}.tbi && #else bcftools index $input_vcf && #end if #elif $input_file.is_of_type('bcf') #set $input_vcf = 'input.bcf' ln -s '$input_file' $input_vcf && #if $input_file.metadata.bcf_index: ln -s '${input_file.metadata.bcf_index}' ${input_vcf}.csi && #else bcftools index $input_vcf && #end if #end if #set $section = $sec_consensus_variant_calling.variant_calling #set $targets_path = None #if $section.method == 'multiallelic': #if $section.genotypes.constrain == 'alleles': #set $section = $sec_consensus_variant_calling.variant_calling.genotypes #set $targets_path = None #if 'targets' in $section #if $section.targets.targets_src == 'targets_file': #set $targets_path = 'targets_file.tab.gz' bgzip -c "$section.targets.targets_file" > $targets_path && tabix -s 1 -b 2 -e 2 $targets_path && #end if #elif $tgts_sec.targets_file: #set $targets_path = 'targets_file.tab.gz' bgzip -c "$section.targets_file" > $targets_path && tabix -s 1 -b 2 -e 2 $targets_path && #end if #end if #end if #set $section = $sec_restrict #set $regions_path = None #if 'regions' in $section #if $section.regions.regions_src == 'regions_file' and $section.regions.regions_file: #if $section.regions.regions_file.ext.startswith('bed'): #set $regions_path = 'regions_file.bed' ln -s '$section.regions.regions_file' $regions_path && #end if #end if #end if bcftools call #set $section = $sec_consensus_variant_calling.variant_calling #if $section.method == 'multiallelic': -m #if str($section.gvcf): --gvcf $section.gvcf #end if #if str($section.prior_freqs): --prior-freqs '$section.prior_freqs' #end if #if str($section.prior): --prior $section.prior #end if #if $section.genotypes.constrain == 'alleles': --constrain alleles $section.genotypes.insert_missed #set $section = $sec_consensus_variant_calling.variant_calling.genotypes #if $targets_path is not None: --targets-file "${section.invert_targets_file}${targets_path}" #elif $section.targets_file: --targets-file "${section.invert_targets_file}${section.targets_file}" #end if #else #if $section.genotypes.constrain == 'trio': --constrain trio #set $novel_rate = [] #if str($section.genotypes.novel_rate_snp): #silent $novel_rate.append(str($section.genotypes.novel_rate_snp)) #end if #if str($section.genotypes.novel_rate_del): #silent $novel_rate.append(str($section.genotypes.novel_rate_del)) #end if #if str($section.genotypes.novel_rate_ins): #silent $novel_rate.append(str($section.genotypes.novel_rate_ins)) #end if #if len($novel_rate) > 0: --novel-rate '#echo ','.join($novel_rate)#' #end if #end if #set $section = $sec_consensus_variant_calling.variant_calling.genotypes #if $targets_path: --targets-file "${section.targets.invert_targets_file}${targets_path}" #elif $section.targets.targets_src == 'targets': #set $intervals = $section.targets.targets #set $components = [] #for $i in $intervals: #set $chrom = str($i.chrom).strip() #set $start = str($i.start).strip() #set $stop = str($i.stop).strip() #if $start or $stop: $components.append($chrom + ':' + ($start or '0') + '-' + $stop) #else: $components.append($chrom) #end if #end for #set $intervals_spec = ','.join($components) --targets '${section.targets.invert_targets_file}$intervals_spec' #elif $section.targets.targets_src == 'targets_file' and $section.targets.targets_file: --targets-file "${section.targets.invert_targets_file}${section.targets.targets_file}" #end if #if $section.targets_overlap --targets-overlap $section.targets_overlap #end if #end if #else -c #if str($section.pval_threshold): --pval-threshold $section.pval_threshold #end if #end if #set $section = $sec_restrict #if $section.regions.regions_src == 'regions': #set $intervals = $section.regions.regions #set $components = [] #for $i in $intervals: #set $chrom = str($i.chrom).strip() #set $start = str($i.start).strip() #set $stop = str($i.stop).strip() #if $start or $stop: $components.append($chrom + ':' + ($start or '0') + '-' + $stop) #else: $components.append($chrom) #end if #end for #set $intervals_spec = ','.join($components) --regions '$intervals_spec' #elif $section.regions.regions_src == 'regions_file' and $section.regions.regions_file: #if $regions_path is not None: --regions-file '$regions_path' #else: --regions-file '$section.regions.regions_file' #end if #end if #if $section.regions_overlap --regions-overlap $section.regions_overlap #end if #set $samples_defined = False #if str($section.samples) != '': #set $samples_defined = True --samples '${section.invert_samples}${section.samples}' #end if #if $section.samples_file: #set $samples_defined = True --samples-file "${section.invert_samples_file}${section.samples_file}" #end if ## File format section #set $section = $sec_file_format #if $section.ploidy: --ploidy ${section.ploidy} #end if #if $section.ploidy_file: --ploidy-file '${section.ploidy_file}' #end if ## Input/output section #set $section = $sec_input_output ${section.group_samples} ${section.keep_alts} #if $section.format_fields: --format-fields '${section.format_fields}' #end if ${section.keep_masked_ref} #if $section.skip_variants: --skip-variants ${section.skip_variants} #end if ${section.variants_only} #if $section.output_tags --annotate $section.output_tags #end if #if str($output_type) != "__none__": --output-type '${output_type}' #end if --threads \${GALAXY_SLOTS:-4} ## Primary Input/Outputs $input_vcf > '$output_file'
Functional tests |
name | inputs | outputs | required files |
Test-1 |
input_file: mpileup.vcf sec_consensus_variant_calling|variant_calling|method: multiallelic sec_input_output|variants_only: True output_type: v |
name: value |
mpileup.vcf value |
Test-2 |
input_file: mpileup.vcf sec_consensus_variant_calling|variant_calling|gvcf: 0 sec_consensus_variant_calling|variant_calling|method: multiallelic output_type: v |
name: value |
mpileup.vcf value |
Test-3 |
input_file: mpileup.X.vcf sec_restrict|samples_file: mpileup.samples sec_consensus_variant_calling|variant_calling|method: multiallelic sec_file_format|ploidy_file: mpileup.ploidy output_type: v |
name: value |
mpileup.X.vcf mpileup.samples mpileup.ploidy value |
Test-4 |
input_file: mpileup.X.vcf sec_consensus_variant_calling|variant_calling|method: consensus sec_file_format|ploidy_file: mpileup.ploidy output_type: v |
name: value |
mpileup.X.vcf mpileup.ploidy value |
Test-5 |
input_file: mpileup.X.vcf sec_consensus_variant_calling|variant_calling|method: consensus sec_file_format|ploidy_file: mpileup.ploidy sec_input_output|output_tags: INFO/PV4 output_type: v |
name: value |
mpileup.X.vcf mpileup.ploidy value |
Test-6 |
input_file: mpileup.vcf sec_restrict|regions_overlap: 1 sec_consensus_variant_calling|variant_calling|method: multiallelic sec_input_output|variants_only: True output_type: v |
name: value |
mpileup.vcf value |
Test-7 |
input_file: mpileup.AD.vcf sec_consensus_variant_calling|variant_calling|method: multiallelic sec_input_output|group_samples: True output_type: v |
name: value |
mpileup.AD.vcf value |