FastQCFastQC Report
Sat 18 Jun 2016
SRR3549576_1.fastq

Summary

[OK]Basic Statistics

MeasureValue
FilenameSRR3549576_1.fastq
File typeConventional base calls
EncodingSanger / Illumina 1.9
Total Sequences1110774
Sequences flagged as poor quality0
Sequence length51
%GC46

[OK]Per base 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

[FAIL]Sequence Duplication Levels

Duplication level graph

[FAIL]Overrepresented sequences

SequenceCountPercentagePossible Source
GAATGATACGGCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGC361063.2505262096520084No Hit
GAATGATACCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCG308292.775452072158693No Hit
GAATCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTC262092.359525880152038No Hit
GCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTGC154471.390651923793679TruSeq Adapter, Index 22 (95% over 22bp)
CCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTGC120721.0868097380745319TruSeq Adapter, Index 22 (95% over 22bp)
GAATGATACGGCGACCACCTGTCTCTTATACACATCTGACGCTCTAGTTGT113901.0254111097306922No Hit
CTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTGCT90210.8121364021844226TruSeq Adapter, Index 20 (95% over 22bp)
GAACTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCT78580.7074346356684618No Hit
GAATGATACGGCGACTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTA77880.701132723668361No Hit
TCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTGC65020.58535759749508TruSeq Adapter, Index 22 (95% over 22bp)
GAATGACTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCT62430.5620405230947069No Hit
GAATGATCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTC61150.5505170268659512No Hit
CGCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTG30100.2709822160043357No Hit
TGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTGCTT30030.27035202480432563TruSeq Adapter, Index 22 (95% over 24bp)
GAATGATACGGCGACCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGT25550.23001978800368034No Hit
CGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT25180.22668877737505558No Hit
GAATGATACGGCCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATG22270.2004908289174936No Hit
GAATGATACGGCGCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTAT18850.16970148743128666No Hit
TTCCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCT16840.15160599725956855No Hit
CGTTTTTTTTCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCC15420.13882211863079258No Hit
TCCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTG15240.13720162697362379No Hit
GAATGATACGGCGACCACCCTGTCTCTTATACACATCTGACGCTCTAGTTG14580.1312598242306716No Hit
TGCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTCTG13990.12594821268772946No Hit
CGTTCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTTC13000.11703550857330115No Hit
GAATGCTGTCTCTTATACACATCTGACGCTCTAGTTGTCGTATGCCGTCTT11350.10218100171592061No Hit

[FAIL]Adapter Content

Adapter graph

[FAIL]Kmer Content

Kmer graph

SequenceCountPValueObs/Exp MaxMax Obs/Exp Position
CGGATCT351.2118835E-745.0000046
AATACCG351.2118835E-745.00000426
GCACGAA253.8907212E-545.09
ATTCGCG207.0331857E-445.014
TCTAGCG253.8907212E-545.01
GCCGATC502.1827873E-1145.09
GCGATAG207.0331857E-445.09
CGAGCAT207.0331857E-445.016
CGGTAAG207.0331857E-445.011
GCTCGAA207.0331857E-445.013
TACCGTG207.0331857E-445.017
TACGGCT41900.043.174227
ACGGCTG42350.042.662348
ATACGGC81400.042.5122876
TGATACG81950.042.39174
GATACGG82200.042.2627755
ATGATAC116900.042.22843
TGCTACG1500.042.0000044
AATGATA116550.041.8918882
GAATGAT123800.041.8012921