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