report_comment: >
This report has been generated by the nf-core/chipseq
analysis pipeline. For information about how to interpret these results, please see the
documentation.
export_plots: true
fn_clean_exts:
- 'fastq.gz'
- '_trimmed'
- '_val'
- 'sorted.bam'
- '.Lb'
- 'mkD'
- 'clN'
- 'mLb'
- '_peaks'
- '_spp'
- '.spp'
module_order:
- fastqc:
name: 'FastQC (library; raw)'
info: 'This section of the report shows FastQC results before adapter trimming.'
path_filters:
- '*_fastqc.zip'
path_filters_exclude:
- '*val*_fastqc.zip'
- '*trimmed_fastqc.zip'
- cutadapt:
name: 'cutadapt (library; trimmed)'
info: 'This section of the report shows the length of trimmed reads by cutadapt.'
path_filters:
- '*_trimming_report.txt'
- fastqc:
name: 'FastQC (library; trimmed)'
info: 'This section of the report shows FastQC results after adapter trimming.'
path_filters:
- '*val*_fastqc.zip'
- '*trimmed_fastqc.zip'
- samtools:
name: 'SAMTools (library)'
info: 'This section of the report shows SAMTools results for individual libraries.'
path_filters:
- '*.Lb.sorted.bam*'
- samtools:
name: 'SAMTools (merged library; unfiltered)'
info: 'This section of the report shows SAMTools results after merging libraries and before filtering.'
path_filters:
- '*mLb.mkD.sorted.bam*'
- preseq:
name: 'Preseq (merged library; unfiltered)'
info: 'This section of the report shows Preseq results after merging libraries and before filtering.'
path_filters:
- '*mLb*'
- samtools:
name: 'SAMTools (merged library; filtered)'
info: 'This section of the report shows SAMTools results after merging libraries and after filtering.'
path_filters:
- '*mLb.clN.sorted.bam*'
- picard:
name: 'Picard (merged library; filtered)'
info: 'This section of the report shows picard results after merging libraries and after filtering.'
path_filters:
- '*mLb*'
- deeptools:
name: 'deepTools'
info: 'This section of the report shows ChIP-seq QC plots generated by deepTools.'
path_filters:
- '*.plot*'
- featureCounts:
name: 'featureCounts'
info: 'This section of the report shows featureCounts results for the number of reads assigned to merged library consensus peaks.'
path_filters:
- '*featureCounts*'
report_section_order:
peak_count:
order: -1000
frip_score:
order: -1100
strand_shift_correlation:
order: -1200
nsc_coefficient:
order: -1300
rsc_coefficient:
order: -1400
peak_annotation:
order: -1500
deseq2_pca_1:
order: -1600
deseq2_pca_2:
order: -1700
deseq2_pca_3:
order: -1800
deseq2_pca_4:
order: -1900
deseq2_pca_5:
order: -2000
deseq2_pca_6:
order: -2100
deseq2_pca_7:
order: -2200
deseq2_pca_8:
order: -2300
deseq2_pca_9:
order: -2400
deseq2_pca_10:
order: -2500
deseq2_clustering_1:
order: -2600
deseq2_clustering_2:
order: -2700
deseq2_clustering_3:
order: -2800
deseq2_clustering_4:
order: -2900
deseq2_clustering_5:
order: -3000
deseq2_clustering_6:
order: -3100
deseq2_clustering_7:
order: -3200
deseq2_clustering_8:
order: -3300
deseq2_clustering_9:
order: -3400
deseq2_clustering_10:
order: -3500
software_versions:
order: -3600
nf-core-chipseq-summary:
order: -3700
custom_plot_config:
picard-insertsize:
cpswitch_c_active: False
smooth_points: 1000
featurecounts:
cpswitch_c_active: False