FastQCFastQC Report
Tue 16 Jan 2018
H5TH7BCX2_l02n02_wt-2.352000000b0db1.fastq.gz

Summary

[OK]Basic Statistics

MeasureValue
FilenameH5TH7BCX2_l02n02_wt-2.352000000b0db1.fastq.gz
File typeConventional base calls
EncodingSanger / Illumina 1.9
Total Sequences26147
Sequences flagged as poor quality0
Sequence length51
%GC52

[OK]Per base sequence quality

Per base quality graph

[WARN]Per tile sequence quality

Per base quality graph

[OK]Per sequence quality scores

Per Sequence quality graph

[FAIL]Per base sequence content

Per base sequence content

[FAIL]Per sequence GC content

Per sequence GC content graph

[OK]Per base N content

N content graph

[OK]Sequence Length Distribution

Sequence length distribution

[OK]Sequence Duplication Levels

Duplication level graph

[FAIL]Overrepresented sequences

SequenceCountPercentagePossible Source
AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG317712.150533522010173Illumina Single End PCR Primer 1 (100% over 51bp)
GTGACTGGAGTTCAGACGTGTGCAGATCGGAAGAGCGTCGTGTAGGGAAAG1960.7496079856197652Illumina Single End PCR Primer 1 (100% over 28bp)
GTGACTGGAGTTCAGACGTGTGCTAGATCGGAAGAGCGTCGTGTAGGGAAA1940.7419589245420125Illumina Single End PCR Primer 1 (100% over 27bp)
GTGACTGGAGTTCAGACGTGTGAGATCGGAAGAGCGTCGTGTAGGGAAAGA1110.4245228898152752Illumina Single End PCR Primer 1 (100% over 29bp)
GTGACTGGAGTTCAGACGTGTGCTCAGATCGGAAGAGCGTCGTGTAGGGAA1100.4206983592763988Illumina Single End PCR Primer 1 (100% over 26bp)
AGATCGGAAGAGCGTCGGGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG1010.3862775844265116Illumina Single End PCR Primer 1 (98% over 51bp)
AGATCGGAAGAGCGTCGTGTAGGGCAAGAGTGTAGATCTCGGTGGTCGCCG950.36333040119325355Illumina Single End PCR Primer 1 (98% over 51bp)
GGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG880.33655868742111905Illumina Single End PCR Primer 1 (98% over 51bp)
GTGACTGGAGTTCAGACGTGTGCTCTTCAGATCGGAAGAGCGTCGTGTAGG820.31361150418786093Illumina Multiplexing PCR Primer 2.01 (96% over 33bp)
AGGTCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG540.20652464909932305Illumina Single End PCR Primer 1 (98% over 51bp)
AGATCTGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG520.19887558802157032Illumina Single End PCR Primer 1 (98% over 51bp)
GTGACTGGAGTTCAGACGTGTGCTCTTGTTAGATCGGAAGAGCGTCGTGTA510.195051057482694Illumina Multiplexing PCR Primer 2.01 (96% over 27bp)
AGATCGGAAGAGCGGCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG420.16063028263280682Illumina Single End PCR Primer 1 (98% over 51bp)
AGAACGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG390.14915669101617776Illumina Single End PCR Primer 1 (98% over 51bp)
AGATCGGAAGAGCGTCGTTTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCG380.1453321604773014Illumina Single End PCR Primer 1 (98% over 51bp)
GTGACTGGAGTTCAGACGTGTGCTCTAGATCGGAAGAGCGTCGTGTAGGGA380.1453321604773014Illumina Multiplexing PCR Primer 2.01 (96% over 26bp)

[FAIL]Adapter Content

Adapter graph

[WARN]Kmer Content

Kmer graph

SequenceCountPValueObs/Exp MaxMax Obs/Exp Position
TGTAGAA253.7256905E-545.12307731
AGGTCGC453.45608E-1045.12307743
TTTAGAT302.04567E-645.12307431
AACCGTG206.8794354E-445.0364726
GGGTAGA302.0730677E-645.0364729
TTCCGAG206.8794354E-445.0364726
TCTGGGT502.0008883E-1145.0364737
CTCGGAG253.7684098E-545.0364738
GGGTGGT502.0008883E-1145.0364740
ATGAGTG502.0008883E-1145.0364726
AATGAGT206.8794354E-445.0364725
CATGAGT351.14467184E-745.03646525
AGCGAGT351.14467184E-745.03646527
GGCATGA206.944983E-444.95019523
GGGCAAC206.944983E-444.95019522
AACTGGA206.944983E-444.9501953
CACGTCA206.944983E-444.95019521
GCGGTTA406.4483174E-944.95019515
GCGGTGA206.944983E-444.95019515
GAACGGG206.944983E-444.9501952