QC Report


general
Report generated at2021-11-23 06:01:28
TitleENCSR138NWM-1
DescriptionNo description
Pipeline versionv1.10.0
Pipeline typeatac
Genomehg38
Alignerbowtie2
Sequencing endedness{'rep1': {'paired_end': True}}
Peak callermacs2

Alignment quality metrics


Fragment length statistics (filtered/deduped BAM)

rep1
Fraction of reads in NFR0.7145900451627022
Fraction of reads in NFR (QC pass)True
Fraction of reads in NFR (QC reason)OK
NFR / mono-nuc reads3.0375551406192076
NFR / mono-nuc reads (QC pass)True
NFR / mono-nuc reads (QC reason)OK
Presence of NFR peakTrue
Presence of Mono-Nuc peakTrue
Presence of Di-Nuc peakTrue

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Open chromatin assays show distinct fragment length enrichments, as the cut sites are only in open chromatin and not in nucleosomes. As such, peaks representing different n-nucleosomal (ex mono-nucleosomal, di-nucleosomal) fragment lengths will arise. Good libraries will show these peaks in a fragment length distribution and will show specific peak ratios.



Sequence quality metrics (filtered/deduped BAM)

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Open chromatin assays are known to have significant GC bias. Please take this into consideration as necessary.


Annotated genomic region enrichment

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Fraction of Reads in universal DHS regions0.5462076578619204
Fraction of Reads in blacklist regions0.008148691900641332
Fraction of Reads in promoter regions0.2278065685539521
Fraction of Reads in enhancer regions0.377580830007028

Signal to noise can be assessed by considering whether reads are falling into known open regions (such as DHS regions) or not. A high fraction of reads should fall into the universal (across cell type) DHS set. A small fraction should fall into the blacklist regions. A high set (though not all) should fall into the promoter regions. A high set (though not all) should fall into the enhancer regions. The promoter regions should not take up all reads, as it is known that there is a bias for promoters in open chromatin assays.


Replication quality metrics


Number of raw peaks

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Number of peaks299248

Top 300000 raw peaks from macs2 with p-val threshold 0.01

Peak calling statistics


Peak region size

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Min size150.0
25 percentile388.0
50 percentile (median)630.0
75 percentile923.0
Max size3320.0
Mean707.248212185211

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Enrichment / Signal-to-noise ratio


Jensen-Shannon distance (filtered/deduped BAM)

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AUC0.1169915525820231
Synthetic AUC0.49757852040375605
X-intercept0.11232942982684103
Synthetic X-intercept0.0
Elbow Point0.8482310278789527
Synthetic Elbow Point0.5038995758478982
Synthetic JS Distance0.594958841850054

Peak enrichment


Fraction of reads in peaks (FRiP)

FRiP for macs2 raw peaks

rep1
Fraction of Reads in Peaks0.5488451811409073

For macs2 raw peaks:


For overlap/IDR peaks: