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output.md

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Output specification

All output filenames keep prefixes from corresponding input filenames. For example. If you have started from REP1.fastq.gz and REP2.fastq.gz then corresponding alignment log for each replicate has a filename of REP1.flagstat.qc and REP2.flagstat.qc, respectively.

Final HTML report (qc.html) and QC json (qc.json) files do not have any prefix.

  1. DNANexus: If you choose to use dxWDL and run pipelines on DNANexus platform, then output will be stored on the specified output directory without any subdirectories.

  2. Cromwell: Otherwise Cromwell will store outputs for each task under cromwell-executions/[WORKFLOW_ID]/call-[TASK_NAME]/shard-[IDX]. For all tasks except idr and overlap, [IDX] means a zero-based index for each replicate but for tasks idr and overlap it stands for a zero-based index for all possible pair of replicates. For example, you have 3 replicates and all possible combination of two replicates are [(rep1,rep2), (rep1,rep3), (rep2,rep3)]. Therefore, call-idr/shard-2 should be an output directory for the pair of replicate 2 and 3.

For more details, refer to the file table section in an HTML report generated by the pipeline. Files marked as (E) are outputs to be uploaded during ENCODE accession.

task filename description
trim_adapter * .trim.fastq.gz adapter-trimmed FASTQ
trim_adapter merge_fastqs_R?_*.fastq.gz Merged and adapter-trimmed FASTQ
bowtie2 * .bam Raw BAM
bowtie2 * .bai BAI for Raw BAM
bowtie2 * .align.log Bowtie2 log for mapping
bowtie2 * .flagstat.qc Samtools flagstat log for raw BAM
filter * .nodup.bam Filtered/deduped BAM
filter * .nodup.flagstat.qc Samtools flagstat log for filtered/deduped BAM
filter * .dup.qc Picard/sambamba markdup log
filter * .pbc.qc PBC QC log
bam2ta * .tagAlign.gz TAG-ALIGN generated from filtered BAM
bam2ta * .N.tagAlign.gz Subsampled (N reads) TAG-ALIGN generated from filtered BAM
bam2ta * .tn5.tagAlign.gz TN5-shifted TAG-ALIGN
spr * .pr1.tagAlign.gz 1st pseudo-replicated TAG-ALIGN
spr * .pr2.tagAlign.gz 2nd pseudo-replicated TAG-ALIGN
pool_ta * .tagAlign.gz Pooled TAG-ALIGN from all replciates
xcor * .cc.plot.pdf Cross-correlation plot PDF
xcor * .cc.plot.png Cross-correlation plot PNG
xcor * .cc.qc Cross-correlation analysis score log
xcor * .cc.fraglen.txt Estimated fragment length
macs2 * .narrowPeak.gz NARROWPEAK
macs2 * .bfilt.narrowPeak.gz Blacklist-filtered NARROWPEAK
macs2 * .pval.signal.bigwig p-val signal BIGWIG
macs2 * .fc.signal.bigwig fold enrichment signal BIGWIG
macs2 * .frip.qc Fraction of read (TAG-ALIGN) in peaks (NARROWPEAK)
idr * .*Peak.gz IDR NARROWPEAK
idr * .bfilt.*Peak.gz Blacklist-filtered IDR NARROWPEAK
idr * .txt.png IDR plot PNG
idr * .txt.gz Unthresholded IDR output
idr * .log IDR STDOUT log
idr * .frip.qc Fraction of read (TAG-ALIGN) in peaks (IDR NARROWPEAK)
overlap * .*Peak.gz Overlapping NARROWPEAK
overlap * .bfilt.*Peak.gz Blacklist-filtered overlapping NARROWPEAK
overlap * .frip.qc Fraction of read (TAG-ALIGN) in peaks (overlapping NARROWPEAK)
reproducibility * .reproducibility.qc Reproducibililty QC log
reproducibility optimal_peak.gz Optimal final peak file
reproducibility conservative_peak.gz Conservative final peak file
qc_report qc.html Final HTML QC report
qc_report qc.json Final QC JSON