of 2
ChipAlignmentEnrichmentQualityMetric
TF, Histone
subsampled_reads
Number of reads subsampled from the sample for calculation of all cross-correlation metrics
estimated_fragment_len
Fragment length/strandshift. This is the estimated fragment length/strand shift for each dataset as estimated by strand shift cross-correlation analysis
corr_estimated_fragment_len
Value of correlation function at estimated fragment length.
phantom_peak
Strand shift value at which the phantom (false) peak in cross-correlation is observed. This is typically the read length.
corr_phantom_peak
Value of cross-correlation function at strand shift corresponding to phantom_peak (which is typically the read length)
argmin_corr
Strand shift corresponding to the minimum value of cross-correlation (min_corr)
min_corr
Minimum cross-correlation over a sufficiently wide range of strand shifts (typically -100 bp to ~3 times the expected size of DNA fragments based on sonication and size selection protocols).
NSC
Normalized strand cross-correlation = FRAGLEN_CC / MIN_CC. Ratio of strand cross-correlation at estimated fragment length to the minimum cross-correlation over all shifts.
RSC
Relative cross-correlation coefficient. Ratio of strand cross-correlation at fragment length and at read length
auc
The “area under the curve”, with a maximum value of 0.5. Lower values generally indicate higher and more focal enrichment.
syn_auc
The expected area under the curve of a perfectly behaved input sample having the same mean sequencing depth of a given sample. This is useful to put the observed AUC into perspective.
x_intercept
The point (on the X-axis) at which the curve is 0. This is approximately the percentage of the genome that was not sequenced in a particular sample.
syn_x_intercept
The expected X-intercept of a perfectly behaved input sample having the same mean sequencing depth of a given sample. This is useful to put the observed X-intercept into perspective.
elbow_pt
The elbow point attempts to measure the position at which the line turns upward. In practice, this is the point at which the plotted line is furthest from the line from the lower-left to the upper-right corner of the graph (equivalent to a perfect input sample with infinite coverage). The point returned is the position on the X-axis of this elbow point and higher values indicate more enrichment.
syn_elbow_pt
The expected elbow point of a perfectly behaved input sample having the same mean sequencing depth of a given sample. This is useful to put the observed elbow point into perspective.
jsd
The Jensen-Shannon distance between the replicate and the control.
syn_jsd
The Jensen-Shannon distance between a given sample and a perfect input sample with the same coverage depth (i.e., the plot generated from the Poisson probability mass function with lambda equal to the mean coverage in the sample).
pct_genome_enrich
The approximate percentage of the genome enriched in signal (e.g., bound by a transcription factor or having a certain histone modification).
diff_enrich
The differential enrichment between a given sample and that indicated by --JSDsample at the elbow point.
ch_div
The CHANCE divergence between the replicate and the control.
ChipAlignmentQualityMetric
TF, Histone
total_reads
Number of total reads passing QC"
total_reads_qc_failed
Number of total reads failing QC
duplicate_reads
Number of reads with duplicates passing QC
duplicate_reads_qc_failed
Number of reads with duplicates failing QC
mapped_reads
Number of mapped reads passing QC
mapped_reads_qc_failed
Number of mapped reads failing QC
pct_mapped_reads
Percent of mapped reads passing QC
paired_reads
Number of paired reads passing QC
paired_reads_qc_failed
Number of paired reads failing QC
read1
Number of read1 reads passing QC
read1_qc_failed
Number of read1 reads failing QC
read2
Number of read2 reads passing QC
read2_qc_failed
Number of read2 reads failing QC
properly_paired_reads
Number of properly paired reads passing QC
properly_paired_reads_qc_failed
Number of properly paired reads failing QC
pct_properly_paired_reads
Percent of properly paired reads passing QC
with_itself
Number of reads with both itself & mate mapped passing QC
with_itself_qc_failed
Number of reads with both itself & mate mapped failing QC
singletons
Number of singletons (unpaired reads) passing QC
singletons_qc_failed
Number of singletons (unpaired reads) failing QC
pct_singletons
Percent of singletons (unpaired reads) passing QC
diff_chroms
Number of reads with mate mapped to different chromosomes passing QC
diff_chroms_qc_failed
Number of reads with mate mapped to different chromosomes failing QC
usable_fragments
Usable fragments, based on the mapped_reads value.
ChipLibraryQualityMetric
TF, Histone
unpaired_reads
Number of unpaired reads before filtering
paired_reads
Number of paired reads before duplicate filtering
unmapped_reads
Number of unmapped reads before duplicate filtering
unpaired_duplicate_reads
Number of unpaired duplicates before duplicate filtering
paired_duplicate_reads
Number of paired duplicates before duplicate filtering
paired_optical_duplicate_reads
Number of paired optical duplicates before duplicate filtering
pct_duplicate_reads
Percent of paired duplicates before duplicate filtering
total_fragments
Number of fragments before duplicate filtering
distinct_fragments
Number of distinct fragments
positions_with_one_read
Number of locations to which exactly one read (pair) maps
NRF
Non redundant fraction (indicates library complexity). Number of distinct unique mapping reads (i.e. after removing duplicates) / Total number of reads
PBC1
PCR Bottlenecking coefficient 1 = M1/M_DISTINCT where M1: number of genomic locations where exactly one read maps uniquely, M_DISTINCT: number of distinct genomic locations to which some read maps uniquely
PBC2
PCR Bottlenecking coefficient 2 (indicates library complexity) = M1/M2 where M1: number of genomic locations where only one read maps uniquely and M2: number of genomic locations where 2 reads map uniquely
ChipPeakEnrichmentQualityMetric
TF, Histone
frip
Fraction of reads in the peak file
min_size
Smallest peak width
25_pct
25th percentile of peak widths
50_pct
50th percentile of peak widths
75_pct
75th percentile of peak widths
max_size
Largest peak width
mean
Mean peak width
ChipReplicationQualityMetric
TF, Histone
reproducible_peaks
Number of peaks called from one replicate or pooled replicates passing reproducibility test by comparing self-pseudoreplicates or pooled pseudo-replicates.
idr_cutoff
Irreproducible Discovery Rate (IDR) threshold used to define reproducible peaks
rescue_ratio
max(Np,Nt) / min (Np,Nt); Np: Pooled-pseudoreplicate consistent peaks (comparing two pseudoreplicates generated by subsampling pooled reads from Rep1 and Rep2); Nt: True Replicate consistent peaks (comparing true replicates Rep1 vs Rep2)
self_consistency_ratio
max(N1,N2) / min (N1,N2); N1: Replicate 1 self-consistent peaks (comparing two pseudoreplicates generated by subsampling Rep1 reads); N2: same as N1 for Rep2
reproducibility
Reproducibility test result for this experiment (pass/fail)
ChipSeqFilterQualityMetric
Deprecated
NSC
Normalized strand cross-correlation = FRAGLEN_CC / MIN_CC. Ratio of strand cross-correlation at estimated fragment length to the minimum cross-correlation over all shifts.
RSC
Relative cross correlation coefficient. Ratio of strand cross-correlation at fragment length and at read length
PBC1
PCR Bottlenecking coefficient 1 = M1/M_DISTINCT where M1: number of genomic locations where exactly one read maps uniquely, M_DISTINCT: number of distinct genomic locations to which some read maps uniquely
PBC2
PCR Bottlenecking coefficient 2 (indicates library complexity) = M1/M2 where M1: number of genomic locations where only one read maps uniquely and M2: number of genomic locations where 2 reads map uniquely
fragment length
Fragment length/strandshift. This is the estimated fragment length/strand shift for each dataset as estimated by strand cross-correlation analysis
NRF
Non redundant fraction (indicates library complexity). Number of distinct unique mapping reads (i.e. after removing duplicates) / Total number of reads
ComplexityXcorrQualityMetric
Deprecated
sample size
Total reads sampled (pairs if applicable)
paired-end
Reads are paired-ended
read length
Read length
fragment length
Fragment length/strandshift. This is the estimated fragment length/strand shift for each dataset as estimated by strand cross-correlation analysis
NRF
Non redundant fraction (indicates library complexity). Distinct Locations Mapped / Sampled Reads
PBC1
PCR Bottlenecking coefficient 1 = Single-read Locations / Distinct Locations
PBC2
PCR Bottlenecking coefficient 2 (indicates library complexity) = Single-read Locations / Multi-read Locations
NSC
Normalized strand cross-correlation = FRAGLEN_CC / MIN_CC. Ratio of strand cross-correlation at estimated fragment length to the minimum cross-correlation over all shifts.
RSC
Relative cross correlation coefficient. Ratio of strand cross-correlation at fragment length and at read length
cross_correlation_plot
Cross-correlation plot
HistoneChipSeqQualityMetric
Deprecated
nreads
# of starting reads in the pool (if replicated) or experiment (if unreplicated)
nreads_in_peaks
# of reads that fall within peaks.
npeak_overlap
# peaks overlapping with true replicate or pooled pseudoreplicate peaks
Fp
Fraction reads in replicated/stable narrowPeaks (FRiP) from pooled pseudoreplicates
Ft
Fraction reads in replicated/stable narrowPeaks (FRiP) from true replicates
F1
Fraction reads in replicated/stable narrowPeaks (FRiP) from replicate 1 self-pseudoreplicates that pass internal pseudoreplication, when self-pseudoreplication is done on unreplicated experiments.
F2
Fraction reads in replicated/stable narrowPeaks (FRiP) from replicate 2 self-pseudoreplicates
frip
Best fraction reads in peaks (FRiP) from peaks
IDRQualityMetric
Deprecated
Fp
Fraction reads in IDR peaks (FRiP) from pooled pseudoreplicates
Ft
Fraction reads in IDR peaks (FRiP) from true replicates
F1
Fraction reads in peaks (FRiP) from replicate 1 self-pseudoreplicates that pass the internal pseudoreplication IDR threshold, when self-pseudoreplication is done on unreplicated experiments.
F2
Fraction reads in peaks (FRiP) from replicate 2 self-pseudoreplicates
Np
Number of peaks from pooled pseudoreplicates
Nt
Number of peaks from true replicates
N1
Number of peaks from replicate 1 self-pseudoreplicates that pass the internal pseudoreplication IDR threshold, when self-pseudoreplication is done on unreplicated experiments.
N2
Number of peaks from replicate 2 self-pseudoreplicates
IDR_cutoff
IDR cutoff threshold for this experiment
self_consistency_ratio
IDR self-consistency ratio for this experiment
rescue_ratio
IDR rescue ratio for this experiment
reproducibility_test
IDR reproducibility test result for this experiment
N_optimal
Number of peaks in the IDR optimal set
N_conservative
Number of peaks in the IDR conservative set
IDR_plot_true
IDR dispersion plot for true replicates
IDR_plot_rep1_pr
IDR dispersion plot for replicate 1 pseudo-replicates
IDR_plot_rep2_pr
IDR dispersion plot for replicate 2 pseudo-replicates
IDR_plot_pool_pr
IDR dispersion plot for pool pseudo-replicates
IDR_parameters_true
IDR run parameters for true replicates
IDR_parameters_rep1_pr
IDR run parameters for replicate 1 pseudo-replicates
IDR_parameters_rep2_pr
IDR run parameters for replicate 2 pseudo-replicates
IDR_parameters_pool_pr
IDR run parameters for pool pseudo-replicates
frip
Fraction reads in IDR peaks (FRiP) from optimal peaks
IdrSummaryQualityMetric
Deprecated
Final parameter values (mu, sigma, rho, and mix)
IDR: Final parameter values (mu, sigma, rho, and mix)
IDR cutoff
IDR: IDR cutoff
Initial parameter values (mu, sigma, rho, and mix)
IDR: Initial parameter values (mu, sigma, rho, and mix)
Number of peaks passing IDR cutoff
IDR: Number of peaks passing IDR cutoff
Number of reported peaks
IDR: Number of reported peaks
Percent peaks passing IDR cutoff
IDR: Percent peaks passing IDR cutoff
Percent reported peaks
IDR: Percent reported peaks