- Selected
- |
- Default Values
- Nested Workflows
- Tools
- Inputs/Outputs
Inputs
ID | Type | Title | Doc |
---|---|---|---|
nthreads | Integer | ||
genome_sizes_file | File |
Genome sizes tab-delimited file (used in samtools) |
|
input_fastq_files | File[] |
Input fastq files |
|
ENCODE_blacklist_bedfile | File |
Bedfile containing ENCODE consensus blacklist regions to be excluded. |
|
genome_ref_first_index_file | File |
Bowtie first index files for reference genome (e.g. *1.ebwt). The rest of the files should be in the same folder. |
Steps
ID | Runs | Label | Doc |
---|---|---|---|
sam2bam |
../map/samtools2bam.cwl
(CommandLineTool)
|
||
bowtie-se |
../map/bowtie-se.cwl
(CommandLineTool)
|
||
sort_bams |
../map/samtools-sort.cwl
(CommandLineTool)
|
||
preseq-c-curve |
../map/preseq-c_curve.cwl
(CommandLineTool)
|
Usage: c_curve [OPTIONS] <sorted-bed-file> |
|
filter-unmapped |
../map/samtools-filter-unmapped.cwl
(CommandLineTool)
|
||
filtered2sorted |
../map/samtools-sort.cwl
(CommandLineTool)
|
||
extract_basename |
../utils/extract-basename.cwl
(CommandLineTool)
|
Extracts the base name of a file |
|
count_fastq_reads |
../utils/count-fastq-reads.cwl
(CommandLineTool)
|
Counts reads in a fastq file |
|
sort_filtered_bam |
../map/samtools-sort.cwl
(CommandLineTool)
|
||
index_filtered_bam |
../map/samtools-index.cwl
(CommandLineTool)
|
||
mapped_reads_count |
../map/bowtie-log-read-count.cwl
(CommandLineTool)
|
Get number of processed reads from Bowtie log. |
|
percent_uniq_reads |
../map/preseq-percent-uniq-reads.cwl
(CommandLineTool)
|
Get number of processed reads from Bowtie log. |
|
filtered_bed_to_bam |
../map/bedtools-bedtobam.cwl
(CommandLineTool)
|
Tool: bedtools bedtobam (aka bedToBam)
Version: v2.25.0
Summary: Converts feature records to BAM format. |
|
filter_pcr_artifacts |
../map/filter-pcr-artifacts.cwl
(Workflow)
|
DNase-seq - map - Filter PCR Artifacts |
|
remove_encode_blacklist |
../map/bedtools-intersect.cwl
(CommandLineTool)
|
Tool: bedtools intersect (aka intersectBed)
Version: v2.25.0
Summary: Report overlaps between two feature files. |
|
execute_pcr_bottleneck_coef |
../map/pcr-bottleneck-coef.cwl
(Workflow)
|
ChIP-seq - map - PCR Bottleneck Coefficients |
|
mapped_filtered_reads_count |
../peak_calling/samtools-extract-number-mapped-reads.cwl
(CommandLineTool)
|
Extract mapped reads from BAM file using Samtools flagstat command |
Outputs
ID | Type | Label | Doc |
---|---|---|---|
output_pbc_files | File[] |
PCR Bottleneck Coeficient files. |
|
output_bowtie_log | File[] |
Bowtie log file. |
|
output_read_count_mapped | File[] |
Read counts of the mapped BAM files |
|
original_fastq_read_count | File[] |
Read counts of the (unprocessed) input fastq files |
|
output_preseq_c_curve_files | File[] |
Preseq c_curve output files. |
|
output_percentage_uniq_reads | File[] |
Percentage of uniq reads from preseq c_curve output |
|
output_data_filtered_bam_files | File[] |
BAM files without PCR artifact reads. |
|
output_read_count_mapped_filtered | File[] |
Read counts of the mapped and filtered BAM files |
https://w3id.org/cwl/view/git/517487e59d240c197fc91f08d20dadca97a9e121/v1.0/DNase-seq_pipeline/01-map-se.cwl