- 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/71146d85ae7f0c562ec0d454fbbb7085a827356e/v1.0/DNase-seq_pipeline/01-map-se.cwl
