Open chromatin assays are known to have significant GC bias. Please take this
into consideration as necessary.
Library complexity quality metrics
Library complexity (filtered non-mito BAM)
rep1
rep2
ctl1
Total Fragments
28934696
9245692
8465082
Distinct Fragments
24172150
8291814
7516478
Positions with Two Read
3334141
729734
656750
NRF = Distinct/Total
0.835404
0.89683
0.887939
PBC1 = OneRead/Distinct
0.837176
0.90132
0.896301
PBC2 = OneRead/TwoRead
6.069434
10.241514
10.258126
Mitochondrial reads are filtered out by default.
The non-redundant fraction (NRF) is the fraction of non-redundant mapped reads
in a dataset; it is the ratio between the number of positions in the genome
that uniquely mapped reads map to and the total number of uniquely mappable
reads. The NRF should be > 0.8. The PBC1 is the ratio of genomic locations
with EXACTLY one read pair over the genomic locations with AT LEAST one read
pair. PBC1 is the primary measure, and the PBC1 should be close to 1.
Provisionally 0-0.5 is severe bottlenecking, 0.5-0.8 is moderate bottlenecking,
0.8-0.9 is mild bottlenecking, and 0.9-1.0 is no bottlenecking. The PBC2 is
the ratio of genomic locations with EXACTLY one read pair over the genomic
locations with EXACTLY two read pairs. The PBC2 should be significantly
greater than 1. See more details at
the ENCODE portal standard for ChIP-Seq pipeline
NRF (non redundant fraction)
PBC1 (PCR Bottleneck coefficient 1)
PBC2 (PCR Bottleneck coefficient 2)
PBC1 is the primary measure. Provisionally
N1: Replicate 1 self-consistent peaks (comparing two pseudoreplicates generated by subsampling Rep1 reads)
N2: Replicate 2 self-consistent peaks (comparing two pseudoreplicates generated by subsampling Rep2 reads)
Ni: Replicate i self-consistent peaks (comparing two pseudoreplicates generated by subsampling RepX reads)
Nt: True Replicate consistent peaks (comparing true replicates Rep1 vs Rep2)
Np: Pooled-pseudoreplicate consistent peaks (comparing two pseudoreplicates generated by subsampling pooled reads from Rep1 and Rep2)
Self-consistency Ratio: max(N1,N2) / min (N1,N2)
Rescue Ratio: max(Np,Nt) / min (Np,Nt)
Reproducibility Test: If Self-consistency Ratio >2 AND Rescue Ratio > 2, then 'Fail' else 'Pass'
Number of raw peaks
rep1
rep2
Number of peaks
106470
74057
Top 300000 raw peaks from spp with FDR 0.01
Peak calling statistics
Peak region size
rep1
rep2
idr_opt
overlap_opt
Min size
116.0
102.0
124.0
124.0
25 percentile
464.0
410.0
450.0
450.0
50 percentile (median)
464.0
410.0
450.0
450.0
75 percentile
464.0
410.0
450.0
450.0
Max size
464.0
410.0
450.0
450.0
Mean
463.9924016154785
409.9737769555883
449.26154672395273
449.9728256380606
rep1rep2idr_optoverlap_opt
Enrichment / Signal-to-noise ratio
Strand cross-correlation measures (trimmed/filtered SE BAM)
rep1
rep2
Number of Subsampled Reads
15000000
9245692
Estimated Fragment Length
145
150
Cross-correlation at Estimated Fragment Length
0.842354860811747
0.76052759693971
Phantom Peak
50
50
Cross-correlation at Phantom Peak
0.8418323
0.7587505
Argmin of Cross-correlation
1500
1500
Minimum of Cross-correlation
0.8357021
0.7508415
NSC (Normalized Strand Cross-correlation coeff.)
1.007961
1.0129
RSC (Relative Strand Cross-correlation coeff.)
1.085246
1.224691
Performed on subsampled (15000000) reads mapped from FASTQs that are trimmed to 50.
Such FASTQ trimming and subsampling reads are for cross-corrleation analysis only.
Untrimmed FASTQs are used for all the other analyses.
NOTE1: For SE datasets, reads from replicates are randomly subsampled to 15000000.
NOTE2: For PE datasets, the first end (R1) of each read-pair is selected and trimmed to 50 the reads are then randomly subsampled to 15000000.
Normalized strand cross-correlation coefficient (NSC) = col9 in outFile
Relative strand cross-correlation coefficient (RSC) = col10 in outFile
Estimated fragment length = col3 in outFile, take the top value
rep1rep2
Jensen-Shannon distance (filtered/deduped BAM)
rep1
rep2
AUC
0.40167028926945036
0.3743612704748631
Synthetic AUC
0.49817763004136484
0.4968912395858738
X-intercept
0.02826812071823756
0.029722172289132563
Synthetic X-intercept
0.0
0.0
Elbow Point
0.45050032955839175
0.5009607126450556
Synthetic Elbow Point
0.49950998721801276
0.5011024876574582
JS Distance
0.040500748941515126
0.07497455114695861
Synthetic JS Distance
0.14775722348977835
0.17901984533549284
% Genome Enriched
39.71618031837338
40.344738051011646
Diff. Enrichment
6.702344928002174
11.195218130314133
CHANCE Divergence
0.056960604455401465
0.09523123568117378
Peak enrichment
Fraction of reads in peaks (FRiP)
FRiP for spp raw peaks
rep1
rep2
rep1-pr1
rep2-pr1
rep1-pr2
rep2-pr2
pooled
pooled-pr1
pooled-pr2
Fraction of Reads in Peaks
0.5172129603690085
0.41314656358242696
0.21537814313642156
0.3180290643774757
0.21459854569957879
0.3146832451649458
0.5108508233325405
0.5030070398904555
0.3304421974635314
FRiP for overlap peaks
rep1_vs_rep2
rep1-pr1_vs_rep1-pr2
rep2-pr1_vs_rep2-pr2
pooled-pr1_vs_pooled-pr2
Fraction of Reads in Peaks
0.3310185492977653
0.12291563851309094
0.15875268294697412
0.28581707081048896
FRiP for IDR peaks
rep1_vs_rep2
rep1-pr1_vs_rep1-pr2
rep2-pr1_vs_rep2-pr2
pooled-pr1_vs_pooled-pr2
Fraction of Reads in Peaks
0.018485923296147077
0.005657771910654789
0.005554860584280745
0.01748655193148392
For spp raw peaks:
repX: Peak from true replicate X
repX-prY: Peak from Yth pseudoreplicates from replicate X
pooled: Peak from pooled true replicates (pool of rep1, rep2, ...)
pooled-pr1: Peak from 1st pooled pseudo replicate (pool of rep1-pr1, rep2-pr1, ...)
pooled-pr2: Peak from 2nd pooled pseudo replicate (pool of rep1-pr2, rep2-pr2, ...)
For overlap/IDR peaks:
repX_vs_repY: Comparing two peaks from true replicates X and Y
repX-pr1_vs_repX-pr2: Comparing two peaks from both pseudoreplicates from replicate X
pooled-pr1_vs_pooled-pr2: Comparing two peaks from 1st and 2nd pooled pseudo replicates
