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super-enhancer.cwl
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super-enhancer.cwl
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cwlVersion: v1.0
class: Workflow
requirements:
- class: StepInputExpressionRequirement
- class: InlineJavascriptRequirement
- class: MultipleInputFeatureRequirement
'sd:upstream':
chipseq_sample:
- "chipseq-se.cwl"
- "chipseq-pe.cwl"
- "trim-chipseq-pe.cwl"
- "trim-chipseq-se.cwl"
chipseq_control:
- "chipseq-se.cwl"
- "chipseq-pe.cwl"
- "trim-chipseq-pe.cwl"
- "trim-chipseq-se.cwl"
inputs:
alias:
type: string
label: "Experiment short name/Alias"
sd:preview:
position: 1
islands_file:
type: File
label: "XLS called peaks file"
'sd:upstreamSource': "chipseq_sample/macs2_called_peaks"
'sd:localLabel': true
format: "http://edamontology.org/format_3468"
doc: "Input XLS file generated by MACS2"
islands_control_file:
type: File?
'sd:upstreamSource': "chipseq_control/macs2_called_peaks"
'sd:localLabel': true
label: "XLS called peaks file (control)"
format: "http://edamontology.org/format_3468"
doc: "Control XLS file generated by MACS2"
bambai_pair:
type: File
'sd:upstreamSource': "chipseq_sample/bambai_pair"
secondaryFiles:
- .bai
label: "Coordinate sorted BAM+BAI files"
format: "http://edamontology.org/format_2572"
doc: "Coordinate sorted BAM file and BAI index file"
annotation_file:
type: File
label: "TSV annotation file"
format: "http://edamontology.org/format_3475"
doc: "TSV annotation file"
chrom_length_file:
type: File
label: "Chromosome length file"
format: "http://edamontology.org/format_2330"
doc: "Chromosome length file"
stitch_distance:
type: int?
default: 20000
label: "Stitching distance"
doc: "Linking distance for stitching"
'sd:layout':
advanced: true
tss_distance:
type: int?
default: 2500
label: "TSS distance"
doc: "Distance from TSS to exclude, 0 = no TSS exclusion"
'sd:layout':
advanced: true
promoter_bp:
type: int?
default: 1000
label: "Promoter distance"
doc: "Promoter distance for gene names assignment"
'sd:layout':
advanced: true
outputs:
png_file:
type: File
label: "ROSE visualization plot"
format: "http://edamontology.org/format_3603"
doc: "Generated by ROSE visualization plot"
outputSource: rename_png/target_file
gene_names_file:
type: File
label: "Gateway Super Enhancer + gene names"
format: "http://edamontology.org/format_3475"
doc: "Gateway Super Enhancer results from ROSE with assigned gene names"
outputSource: add_island_names/output_file
bigbed_file:
type: File
label: "Gateway Super Enhancer bigBed file"
format: "http://edamontology.org/format_3475"
doc: "Gateway Super Enhancer bigBed file"
outputSource: bed_to_bigbed/bigbed_file
steps:
make_gff:
run: ../tools/makegff.cwl
in:
islands_file: islands_file
islands_control_file: islands_control_file
out: [gff_file]
run_rose:
run: ../tools/rose.cwl
in:
binding_sites_file: make_gff/gff_file
bam_file: bambai_pair
annotation_file: annotation_file
stitch_distance: stitch_distance
tss_distance: tss_distance
out: [plot_points_pic, gateway_super_enhancers_bed]
rename_png:
in:
source_file: run_rose/plot_points_pic
target_filename:
source: bambai_pair
valueFrom: $(self.location.split('/').slice(-1)[0].split('.').slice(0,-1).join('.')+"_default_s_enhcr.png")
out: [target_file]
run:
cwlVersion: v1.0
class: CommandLineTool
requirements:
- class: DockerRequirement
dockerPull: biowardrobe2/scidap:v0.0.3
inputs:
source_file:
type: File
inputBinding:
position: 5
doc: source file to rename
target_filename:
type: string
inputBinding:
position: 6
doc: filename to rename to
outputs:
target_file:
type: File
outputBinding:
glob: "*"
baseCommand: ["cp"]
doc: Tool renames (copy) `source_file` to `target_filename`
sort_bed:
run: ../tools/linux-sort.cwl
in:
unsorted_file: run_rose/gateway_super_enhancers_bed
key:
default: ["1,1","2,2n","3,3n"]
out: [sorted_file]
reduce_bed:
in:
input_file: sort_bed/sorted_file
out: [output_file]
run:
cwlVersion: v1.0
class: CommandLineTool
requirements:
- class: DockerRequirement
dockerPull: biowardrobe2/scidap:v0.0.3
inputs:
input_file:
type: File
inputBinding:
position: 5
doc: Input BED6 file to be reduced to BED4
outputs:
output_file:
type: File
outputBinding:
glob: "*"
baseCommand: [bash, '-c']
arguments:
- cat $0 | cut -f 1-4 > `basename $0`
doc: Tool converts BED6 to BED4 by reducing column numbers
bed_to_bigbed:
in:
input_bed: reduce_bed/output_file
chrom_length_file: chrom_length_file
bed_type:
default: "bed4"
output_filename:
source: bambai_pair
valueFrom: $(self.location.split('/').slice(-1)[0].split('.').slice(0,-1).join('.')+"_default_s_enhcr.bb")
out: [bigbed_file]
run:
cwlVersion: v1.0
class: CommandLineTool
requirements:
- class: DockerRequirement
dockerPull: biowardrobe2/ucscuserapps:v358
inputs:
bed_type:
type: string
inputBinding:
position: 5
prefix: -type=
separate: false
doc: Type of BED file in a form of bedN[+[P]]. By default bed3 to three required BED fields
input_bed:
type: File
inputBinding:
position: 6
doc: Input BED file
chrom_length_file:
type: File
inputBinding:
position: 7
doc: Chromosome length files
output_filename:
type: string
inputBinding:
position: 8
doc: Output filename
outputs:
bigbed_file:
type: File
outputBinding:
glob: "*"
baseCommand: ["bedToBigBed"]
doc: Tool converts bed to bigBed
bed_to_macs:
in:
input_file: sort_bed/sorted_file
out: [output_file]
run:
cwlVersion: v1.0
class: CommandLineTool
requirements:
- class: DockerRequirement
dockerPull: biowardrobe2/scidap:v0.0.3
inputs:
input_file:
type: File
inputBinding:
position: 5
doc: Input file to be converted to MACS2 output format
outputs:
output_file:
type: File
outputBinding:
glob: "*"
baseCommand: [bash, '-c']
arguments:
- cat $0 | grep -v "#" | awk
'BEGIN {print "chr\tstart\tend\tlength\tabs_summit\tpileup\t-log10(pvalue)\tfold_enrichment\t-log10(qvalue)\tname"}
{print $1"\t"$2"\t"$3"\t"$3-$2+1"\t0\t0\t0\t0\t0\t"$4}' > `basename $0`
doc: Tool converts `input_file` to the format compatible with the input of iaintersect from `assign_genes` step
assign_genes:
run: ../tools/iaintersect.cwl
in:
input_filename: bed_to_macs/output_file
annotation_filename: annotation_file
promoter_bp: promoter_bp
out: [result_file]
add_island_names:
in:
input_file: [assign_genes/result_file, sort_bed/sorted_file]
param:
source: bambai_pair
valueFrom: $(self.location.split('/').slice(-1)[0].split('.').slice(0,-1).join('.')+"_default_s_enhcr.tsv")
out: [output_file]
run:
cwlVersion: v1.0
class: CommandLineTool
requirements:
- class: DockerRequirement
dockerPull: biowardrobe2/scidap:v0.0.3
inputs:
input_file:
type: File[]
inputBinding:
position: 5
doc: TSV file to add extra columns too
param:
type: string
inputBinding:
position: 6
doc: Param to set output filename
outputs:
output_file:
type: File
outputBinding:
glob: "*"
baseCommand: [bash, '-c']
arguments:
- echo -e "refseq_id\tgene_id\ttxStart\ttxEnd\tstrand\tchrom\tstart\tend\tlength\tregion\tname\tscore" > `basename $2`;
cat $0 | grep -v refseq_id | paste - $1 | cut -f 1-9,15,19,20 >> `basename $2`
$namespaces:
s: http://schema.org/
$schemas:
- http://schema.org/docs/schema_org_rdfa.html
s:name: "Super-enhancer post ChIP-Seq analysis"
label: "Super-enhancer post ChIP-Seq analysis"
s:alternateName: "Super Enhancer Analysis by Richard A. Young"
s:downloadUrl: https://raw.githubusercontent.com/datirium/workflows/master/workflows/super-enhancer.cwl
s:codeRepository: https://github.com/datirium/workflows
s:license: http://www.apache.org/licenses/LICENSE-2.0
s:isPartOf:
class: s:CreativeWork
s:name: Common Workflow Language
s:url: http://commonwl.org/
s:creator:
- class: s:Organization
s:legalName: "Cincinnati Children's Hospital Medical Center"
s:location:
- class: s:PostalAddress
s:addressCountry: "USA"
s:addressLocality: "Cincinnati"
s:addressRegion: "OH"
s:postalCode: "45229"
s:streetAddress: "3333 Burnet Ave"
s:telephone: "+1(513)636-4200"
s:logo: "https://www.cincinnatichildrens.org/-/media/cincinnati%20childrens/global%20shared/childrens-logo-new.png"
s:department:
- class: s:Organization
s:legalName: "Allergy and Immunology"
s:department:
- class: s:Organization
s:legalName: "Barski Research Lab"
s:member:
- class: s:Person
s:name: Michael Kotliar
s:email: mailto:misha.kotliar@gmail.com
s:sameAs:
- id: http://orcid.org/0000-0002-6486-3898
doc: |
Super-enhancers, consist of clusters of enhancers that are densely occupied by the master regulators and Mediator.
Super-enhancers differ from typical enhancers in size, transcription factor density and content, ability to activate transcription,
and sensitivity to perturbation.
Use to create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam) given a file of previously identified constituent enhancers (.gff)