Workflow Type: Galaxy

This workflow take as input a collection of paired fastq. It will remove bad quality and adapters with cutadapt. Map with Bowtie2 end-to-end. Will remove reads on MT and unconcordant pairs and pairs with mapping quality below 30 and PCR duplicates. Will compute the pile-up on 5' +- 100bp. Will call peaks and count the number of reads falling in the 1kb region centered on the summit. Will plot the number of reads for each fragment length.

Inputs

ID Name Description Type
PE fastq input #main/PE fastq input Should be a paired collection with ATAC-seq fastqs
  • array containing
    • File
bin_size #main/bin_size Bin size for normalized bigwig (usually 50bp is sufficient)
  • int
effective_genome_size #main/effective_genome_size Used by macs2:\nH. sapiens: 2700000000, M. musculus: 1870000000, D. melanogaster: 120000000, C. elegans: 90000000
  • int
reference_genome #main/reference_genome reference_genome
  • string

Steps

ID Name Description
4 Cutadapt (remove adapter + bad quality bases) toolshed.g2.bx.psu.edu/repos/lparsons/cutadapt/cutadapt/4.9+galaxy1
5 Bowtie2 map on reference toolshed.g2.bx.psu.edu/repos/devteam/bowtie2/bowtie2/2.5.3+galaxy1
6 filter MAPQ30 concordant pairs and not mitochondrial pairs toolshed.g2.bx.psu.edu/repos/devteam/bamtools_filter/bamFilter/2.5.2+galaxy2
7 Get number of reads per chromosome toolshed.g2.bx.psu.edu/repos/devteam/samtools_idxstats/samtools_idxstats/2.0.5
8 remove PCR duplicates toolshed.g2.bx.psu.edu/repos/devteam/picard/picard_MarkDuplicates/3.1.1.0
9 reads in chrM/MT for multiQC toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_awk_tool/9.3+galaxy1
10 convert BAM to BED to improve peak calling toolshed.g2.bx.psu.edu/repos/iuc/bedtools/bedtools_bamtobed/2.31.1+galaxy0
11 Compute fragment length histogram toolshed.g2.bx.psu.edu/repos/iuc/pe_histogram/pe_histogram/1.0.1
12 number of reads toolshed.g2.bx.psu.edu/repos/iuc/samtools_view/samtools_view/1.20+galaxy3
13 Call Peak with MACS2 toolshed.g2.bx.psu.edu/repos/iuc/macs2/macs2_callpeak/2.2.9.1+galaxy0
14 remove comments lines toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_grep_tool/9.3+galaxy1
15 compute 1/million reads toolshed.g2.bx.psu.edu/repos/devteam/column_maker/Add_a_column1/2.1
16 Bigwig from MACS2 (no norm) wig_to_bigWig
17 get summits +/-500kb toolshed.g2.bx.psu.edu/repos/iuc/bedtools/bedtools_slopbed/2.31.1+galaxy0
18 summary of MACS2 toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_grep_tool/9.3+galaxy1
19 Convert 1/million reads to parameter param_value_from_file
20 Isolate each bigwig do normalize not average __APPLY_RULES__
21 Merge summits +/-500kb toolshed.g2.bx.psu.edu/repos/iuc/bedtools/bedtools_mergebed/2.31.1
22 normalize by million reads toolshed.g2.bx.psu.edu/repos/bgruening/deeptools_bigwig_average/deeptools_bigwig_average/3.5.4+galaxy0
23 Compute coverage on summits +/-500kb toolshed.g2.bx.psu.edu/repos/iuc/bedtools/bedtools_coveragebed/2.31.1+galaxy0
24 number of reads in peaks toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_awk_tool/9.3+galaxy1
25 compute 1/million reads in peaks toolshed.g2.bx.psu.edu/repos/devteam/column_maker/Add_a_column1/2.1
26 Combine number of reads in peaks with total number of reads cat1
27 Convert 1/million reads in peaks to parameter param_value_from_file
28 reads in peaks multiQC toolshed.g2.bx.psu.edu/repos/bgruening/text_processing/tp_awk_tool/9.3+galaxy1
29 normalize by million reads in peaks Isolate each bigwig do normalize not average toolshed.g2.bx.psu.edu/repos/bgruening/deeptools_bigwig_average/deeptools_bigwig_average/3.5.4+galaxy0
30 MultiQC toolshed.g2.bx.psu.edu/repos/iuc/multiqc/multiqc/1.24.1+galaxy0

Outputs

ID Name Description Type
1kb around summits #main/1kb around summits n/a
  • File
BAM filtered rmDup #main/BAM filtered rmDup n/a
  • File
Coverage from MACS2 (bigwig) #main/Coverage from MACS2 (bigwig) n/a
  • File
MACS2 narrowPeak #main/MACS2 narrowPeak n/a
  • File
MACS2 report #main/MACS2 report n/a
  • File
MarkDuplicates metrics #main/MarkDuplicates metrics n/a
  • File
MultiQC on input dataset(s): Stats #main/MultiQC on input dataset(s): Stats n/a
  • File
MultiQC webpage #main/MultiQC webpage n/a
  • File
Nb of reads in summits +-500bp #main/Nb of reads in summits +-500bp n/a
  • File
bigwig_norm #main/bigwig_norm n/a
  • File
bigwig_norm2 #main/bigwig_norm2 n/a
  • File
histogram of fragment length #main/histogram of fragment length n/a
  • File
mapping stats #main/mapping stats n/a
  • File

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help Creators and Submitter
Creator
  • Lucille Delisle
Additional credit

Lucille Delisle

Submitter
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Views: 21046   Downloads: 46720   Runs: 3

Created: 21st Oct 2022 at 03:01

Last updated: 17th Jan 2023 at 03:01

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