QC Report

	general
Report generated at	2019-11-29 14:56:52
Title	AWRI1631--MGA2
Description	chipseq of yeast AWRI1631 for tf MGA2
Pipeline version	v1.3.3
Pipeline type	tf
Genome	AWRI1631
Paired-end per replicate	[True, True]
Aligner	bowtie2
Peak caller	spp
Control paired-end per replicate	[True, True, True, True]

Alignment quality metrics

SAMstat (raw unfiltered BAM)

	rep1	rep2	ctl1	ctl2	ctl3	ctl4
Total Reads	3471920	3743620	5917546	6601090	11652572	8804978
Total Reads (QC-failed)	0	0	0	0	0	0
Duplicate Reads	0	0	0	0	0	0
Duplicate Reads (QC-failed)	0	0	0	0	0	0
Mapped Reads	2824697	3086155	4977004	5788309	9693515	6321027
Mapped Reads (QC-failed)	0	0	0	0	0	0
% Mapped Reads	81.39999999999999	82.39999999999999	84.1	87.7	83.2	71.8
Paired Reads	3471920	3743620	5917546	6601090	11652572	8804978
Paired Reads (QC-failed)	0	0	0	0	0	0
Read1	1735960	1871810	2958773	3300545	5826286	4402489
Read1 (QC-failed)	0	0	0	0	0	0
Read2	1735960	1871810	2958773	3300545	5826286	4402489
Read2 (QC-failed)	0	0	0	0	0	0
Properly Paired Reads	2266092	2509464	3717114	4357276	7216522	3826466
Properly Paired Reads (QC-failed)	0	0	0	0	0	0
% Properly Paired Reads	65.3	67.0	62.8	66.0	61.9	43.5
With itself	2775244	3031416	4894834	5693772	9527698	5338574
With itself (QC-failed)	0	0	0	0	0	0
Singletons	49453	54739	82170	94537	165817	982453
Singletons (QC-failed)	0	0	0	0	0	0
% Singleton	1.4000000000000001	1.5	1.4000000000000001	1.4000000000000001	1.4000000000000001	11.200000000000001
Diff. Chroms	1036	1296	2445	2633	5103	2765
Diff. Chroms (QC-failed)	0	0	0	0	0	0

Marking duplicates (filtered BAM)

	rep1	rep2	ctl1	ctl2	ctl3	ctl4
Unpaired Reads	0	0	0	0	0	0
Paired Reads	681552	803419	1618488	1908814	3134719	1665993
Unmapped Reads	0	0	0	0	0	0
Unpaired Duplicate Reads	0	0	0	0	0	0
Paired Duplicate Reads	7449	14152	4666	7580	17416	5903
Paired Optical Duplicate Reads	221	218	658	501	1171	1570
% Duplicate Reads	1.0929	1.7614999999999998	0.2883	0.39709999999999995	0.5556	0.3543

Filtered out (samtools view -F 1804):

read unmapped (0x4)
mate unmapped (0x8, for paired-end)
not primary alignment (0x100)
read fails platform/vendor quality checks (0x200)
read is PCR or optical duplicate (0x400)

SAMstat (filtered/deduped BAM)

	rep1	rep2	ctl1	ctl2	ctl3	ctl4
Total Reads	1348206	1578534	3227644	3802468	6234606	3320180
Total Reads (QC-failed)	0	0	0	0	0	0
Duplicate Reads	0	0	0	0	0	0
Duplicate Reads (QC-failed)	0	0	0	0	0	0
Mapped Reads	1348206	1578534	3227644	3802468	6234606	3320180
Mapped Reads (QC-failed)	0	0	0	0	0	0
% Mapped Reads	100.0	100.0	100.0	100.0	100.0	100.0
Paired Reads	1348206	1578534	3227644	3802468	6234606	3320180
Paired Reads (QC-failed)	0	0	0	0	0	0
Read1	674103	789267	1613822	1901234	3117303	1660090
Read1 (QC-failed)	0	0	0	0	0	0
Read2	674103	789267	1613822	1901234	3117303	1660090
Read2 (QC-failed)	0	0	0	0	0	0
Properly Paired Reads	1348206	1578534	3227644	3802468	6234606	3320180
Properly Paired Reads (QC-failed)	0	0	0	0	0	0
% Properly Paired Reads	100.0	100.0	100.0	100.0	100.0	100.0
With itself	1348206	1578534	3227644	3802468	6234606	3320180
With itself (QC-failed)	0	0	0	0	0	0
Singletons	0	0	0	0	0	0
Singletons (QC-failed)	0	0	0	0	0	0
% Singleton	0.0	0.0	0.0	0.0	0.0	0.0
Diff. Chroms	0	0	0	0	0	0
Diff. Chroms (QC-failed)	0	0	0	0	0	0

Filtered and duplicates removed

Sequence quality metrics (filtered/deduped BAM)

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	ctl2	ctl3	ctl4
Total Fragments	679185	799815	1571325	1852755	3044551	1629062
Distinct Fragments	671789	785768	1567386	1846120	3029617	1623881
Positions with Two Read	7116	13325	3865	6528	14432	5101
NRF = Distinct/Total	0.98911	0.982437	0.997493	0.996419	0.995095	0.99682
PBC1 = OneRead/Distinct	0.989203	0.982595	0.997511	0.996436	0.995157	0.996835
PBC2 = OneRead/TwoRead	93.386172	57.943114	404.523674	281.792279	208.906943	317.337973

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

0-0.5 is severe bottlenecking
0.5-0.8 is moderate bottlenecking
0.8-0.9 is mild bottlenecking
0.9-1.0 is no bottlenecking

Replication quality metrics

IDR (Irreproducible Discovery Rate) plots

Reproducibility QC and peak detection statistics

	overlap	idr
Nt	1489	453
N1	1755	435
N2	1494	442
Np	1561	458
N optimal	1561	458
N conservative	1489	453
Optimal Set	pooled-pr1_vs_pooled-pr2	pooled-pr1_vs_pooled-pr2
Conservative Set	rep1_vs_rep2	rep1_vs_rep2
Rescue Ratio	1.048354600402955	1.011037527593819
Self Consistency Ratio	1.1746987951807228	1.0160919540229885
Reproducibility Test	pass	pass

Reproducibility QC

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	5443	3748

Top 300000 raw peaks from spp with FDR 0.01

Peak calling statistics

Peak region size

	rep1	rep2	idr_opt	overlap_opt
Min size	82.0	82.0	85.0	85.0
25 percentile	316.0	330.0	289.0	340.0
50 percentile (median)	316.0	330.0	321.0	340.0
75 percentile	316.0	330.0	342.75	340.0
Max size	591.0	634.0	737.0	737.0
Mean	311.10821238287707	324.3151013874066	315.1834061135371	332.2075592568866

Enrichment / Signal-to-noise ratio

Strand cross-correlation measures (trimmed/filtered SE BAM)

	rep1	rep2
Number of Subsampled Reads	873786	996910
Estimated Fragment Length	130	135
Cross-correlation at Estimated Fragment Length	0.72361851850502	0.742357245391753
Phantom Peak	55	55
Cross-correlation at Phantom Peak	0.7128152	0.7306089
Argmin of Cross-correlation	1500	1500
Minimum of Cross-correlation	0.6682843	0.6864055
NSC (Normalized Strand Cross-correlation coeff.)	1.0828	1.081514
RSC (Relative Strand Cross-correlation coeff.)	1.242604	1.26578

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

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	0.3520923360376678	0.30102677547648643	0.38295426225033524	0.366967874030114	0.38940546089464206	0.35294691523516786	0.4522861613945892	0.32769794693352067	0.3270025038131215

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	0.1962029425230803	0.19920397921385902	0.2017663224232104	0.19935388862693645

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	0.1430478962941703	0.13219270645583836	0.14489393323172006	0.14335369728776728

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