QC Report


general
Report generated at2019-07-23 08:19:39
TitleENCSR936XTK
DescriptionZNF143 ChIP-seq on human GM12878
Pipeline versionv1.2.2
Genomehg38_google.tsv
Paired-end per replicate[True, True]
Alignerbowtie2
Peak callerspp
Control paired-end per replicate[True, True]

Alignment quality metrics


SAMstat (raw BAM)

rep1rep2ctl1ctl2
Total69122852865903869075305486825372
Total(QC-failed)0000
Dupes0000
Dupes(QC-failed)0000
Mapped68246710839901258949372385502393
Mapped(QC-failed)0000
% Mapped0.00.00.00.0
Paired69122852865903869075305486825372
Paired(QC-failed)0000
Read134561426432951934537652743412686
Read1(QC-failed)0000
Read234561426432951934537652743412686
Read2(QC-failed)0000
Properly Paired67838132834345968852129284602752
Properly Paired(QC-failed)0000
% Properly Paired0.00.00.00.0
With itself67928558835875788890678484921146
With itself(QC-failed)0000
Singletons318152402547586939581247
Singletons(QC-failed)0000
% Singleton0.00.00.00.0
Diff. Chroms3296645352143326123769
Diff. Chroms (QC-failed)0000

Marking duplicates (filtered BAMs)

rep1rep2ctl1ctl2
Unpaired Reads0000
Paired Reads29153381354949913793007636107762
Unmapped Reads0000
Unpaired Dupes0000
Paired Dupes3532920270985538941033874385
Paired Opt. Dupes85622427585258111
% Dupes/1000.1211840.0763450.1026650.107301

Filtered out (samtools view -F 1804):


Fraction of mitochondrial reads

rep1rep2ctl1ctl2
Total reads98395238124526452130195163125019035
Mito. reads45872629252810939521236326
Frac. of mito. reads0.00466207521140.002349123381430.008402401247430.00988910208753
Total deduped reads51240922655702726807194664466754
Mito. deduped reads9862073860214618230650
Frac. of deduped mito. reads0.001924633596560.001126425097030.003152811291750.00357781314691
Total dup reads7065840541971077882067748770
Mito. dup reads20240104684530455862
Frac. of mito. dup reads0.002864486034220.001931468657920.005817000731620.00720914416094

SAMstat (filtered/deduped BAM)

rep1rep2ctl1ctl2
Total51240922655702726807194664466754
Total(QC-failed)0000
Dupes0000
Dupes(QC-failed)0000
Mapped51240922655702726807194664466754
Mapped(QC-failed)0000
% Mapped100.0100.0100.0100.0
Paired51240922655702726807194664466754
Paired(QC-failed)0000
Read125620461327851363403597332233377
Read1(QC-failed)0000
Read225620461327851363403597332233377
Read2(QC-failed)0000
Properly Paired51240922655702726807194664466754
Properly Paired(QC-failed)0000
% Properly Paired100.0100.0100.0100.0
With itself51240922655702726807194664466754
With itself(QC-failed)0000
Singletons0000
Singletons(QC-failed)0000
% Singleton0.00.00.00.0
Diff. Chroms0000
Diff. Chroms (QC-failed)0000

Filtered and duplicates removed


Library complexity quality metrics


Library complexity (filtered non-mito BAM)

rep1rep2ctl1ctl2
Total Reads (Pairs)29093951354528273780011535964506
Distinct Reads (Pairs)25571156327482223392868232118090
One Read (Pair)22431335302357033066118128681729
Two Reads (Pairs)2796921233410328682893078099
NRF = Distinct/Total0.8789170.9237130.8975810.89305
PBC1 = OnePair/Distinct0.8772120.9232780.9036950.893009
PBC2 = OnePair/TwoPair8.0200112.95388510.6897119.318001

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.


NRF (non redundant fraction)
PBC1 (PCR Bottleneck coefficient 1)
PBC2 (PCR Bottleneck coefficient 2)
PBC1 is the primary measure. Provisionally


Alignment enrichment


Strand cross-correlation measures

rep1rep2
Reads1500000015000000
Est. Fragment Len.220215
Corr. Est. Fragment Len.0.2532195583740.238839459296
Phantom Peak5050
Corr. Phantom Peak0.2417820.2503202
Argmin. Corr.15001500
Min. Corr.0.16816720.1863845
NSC1.5057611.281434
RSC1.155370.8204334


Performed on subsampled reads

NOTE1: For SE datasets, reads from replicates are randomly subsampled.
NOTE2: For PE datasets, the first end of each read-pair is selected and the reads are then randomly subsampled.


rep1
rep1
rep2
rep2

Fingerprint and Jensen-Shannon distance

rep1rep2
% genome enriched0.240119298330.267542440612
AUC0.4950978373530.495669896341
CHANCE divergence0.1509641432670.142029449104
Elbow Point0.00.0
JS Distance0.6457410758020.603314773534
Synthetic AUC0.5005838874580.505881863464
Synthetic Elbow Point0.2191146979140.172191362831
Synthetic JS Distance0.3523565342040.306843306467