FastQCFastQC Report
Fri 10 Feb 2017
ERR1631211.fastq

Summary

[OK]Basic Statistics

MeasureValue
FilenameERR1631211.fastq
File typeConventional base calls
EncodingSanger / Illumina 1.9
Total Sequences534314
Sequences flagged as poor quality0
Sequence length43
%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
CTTATACACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGT165233.0923763929075414No Hit
ATACACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTATG148172.773088483550871No Hit
TCTCCGAGCCCACGAGACAAGAGGCAATCTCGTATGCCGTCTT130812.448185898179722RNA PCR Primer, Index 33 (95% over 22bp)
ACACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTATGCC84281.5773496483341258No Hit
CATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTATGCCGTC46240.8654087296982672No Hit
CTCCGAGCCCACGAGACAAGAGGCAATCTCGTATGCCGTCTTC44740.8373353496258754RNA PCR Primer, Index 33 (95% over 23bp)
TATCAACGCAGAGTACTTTTTTTTTTTTTTTTTTTTTTTTTTT37770.7068877102228277No Hit
GTATCAACGCAGAGTACTTTTTTTTTTTTTTTTTTTTTTTTTT36400.6812473564233765No Hit
CACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTATGCCG21060.3941502562163821No Hit
GTACTGGTTCACTATCGGTCAGTCAGGAGTATTTAGCCTTGGA17400.3256512088397459No Hit
GGTATCAACGCAGAGTACTTTTTTTTTTTTTTTTTTTTTTTTT13580.2541576675887212No Hit
TTATACACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTA13320.24929161504283998No Hit
TATACACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTAT12210.22851731378927No Hit
ATCATTAACTGAATCCATAGGTTAATGAGGCGAACCGGGGGAA10940.2047485186613115No Hit
ATACAGGGTGACAGCCCCGTACACAAAAATGCACATGCTGTGA10720.20063108958402737No Hit
ACATCTCCGAGCCCACGAGACAAGAGGCAATCTCGTATGCCGT10150.18996320515651843No Hit
TATTCAGACAGGATACCACGTGTCCCGCCCTACTCATCGAGCT9750.18247697047054728No Hit
GTATTTAGCCTTGGAGGATGGTCCCCCCATATTCAGACAGGAT7870.14729166744648278No Hit
GGATACCACGTGTCCCGCCCTACTCATCGAGCTCACAGCATGT7590.14205130316630296No Hit
CTATCGGTCAGTCAGGAGTATTTAGCCTTGGAGGATGGTCCCC7590.14205130316630296No Hit
CCCATATTCAGACAGGATACCACGTGTCCCGCCCTACTCATCG7400.13849534169046665No Hit
GTATTAGAGGCACCGCCTGCCCAGTGACACATGTTTAACGGCC7320.13699809475327243No Hit
TCACGGTACTGGTTCACTATCGGTCAGTCAGGAGTATTTAGCC6960.13026048353589836No Hit
GTCAGGAGTATTTAGCCTTGGAGGATGGTCCCCCCATATTCAG6850.1282017689972563No Hit
GTATGAATGGCTCCACGAGGGTTCAGCTGTCTCTTACTTTTAA6400.11977975497553872No Hit
GTACATGCTAAGACTTCACCAGTCAAAGCGAACTACTATACTC6280.11753388456974738No Hit
TTATTACCCTCACTGTCAACCCAACACAGGCATGCTCATAAGG6150.11510085829680675No Hit
ACTATACTCAATTGATCCAATAACTTGACCAACGGAACAAGTT5570.10424581800214856No Hit

[OK]Adapter Content

Adapter graph

[FAIL]Kmer Content

Kmer graph

SequenceCountPValueObs/Exp MaxMax Obs/Exp Position
AGCAACG355.623788E-737.02
GCTCTAG308.303656E-637.01
CGTCTTC5400.035.28703737
GATTACG603.45608E-1133.9166681
CTTATAC18450.033.5907861
CGCCGAG507.3159754E-933.3000032
TTATACA18700.032.9438482
ACAGACA451.0781332E-732.8888917
CCTAGTG303.596923E-430.83333417
TAGTGTC303.596923E-430.83333419
AGTGTCC303.596923E-430.83333420
TATACAC20400.030.5612743
ACTTGGT250.00549374429.616
TCCCTTT250.00549374429.637
CAGACAC502.7161695E-729.618
GGTATTG405.9342732E-527.7533
CCGTCTT20100.027.059737
CGGATCG556.251212E-726.9090937
GCCGTCT20550.026.46715236
GTAGCTT358.8631565E-426.42857235