FastQCFastQC Report
Sat 14 Jan 2017
SRR2933799.fastq

Summary

[OK]Basic Statistics

MeasureValue
FilenameSRR2933799.fastq
File typeConventional base calls
EncodingSanger / Illumina 1.9
Total Sequences465626
Sequences flagged as poor quality0
Sequence length51
%GC47

[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
GAATGATACGGCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGC147773.173577076881445No Hit
GAATGATACCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCG123172.6452560638795943No Hit
GAATCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTC110252.367780149733907No Hit
GCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTGC83011.7827612719221004TruSeq Adapter, Index 22 (95% over 22bp)
CCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTGC56771.2192188580534593TruSeq Adapter, Index 22 (95% over 22bp)
GAATGATACGGCGACCACCTGTCTCTTATACACATCTGACGCCGGAGTTAT47871.0280783289592934No Hit
CTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTGCT46591.0005884551120428Illumina Paired End PCR Primer 2 (95% over 21bp)
TCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTGC39030.8382263877017176TruSeq Adapter, Index 22 (95% over 22bp)
GAACTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCT36790.7901191084690288No Hit
GAATGATACGGCGACTGTCTCTTATACACATCTGACGCCGGAGTTATCGTA31560.6777972020462775No Hit
GAATGATCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTC27820.5974752268988416No Hit
GAATGACTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCT25850.5551665929308072No Hit
TGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTGCTT14900.3199993127531538TruSeq Adapter, Index 22 (95% over 24bp)
GAATGATACGGCGACCTGTCTCTTATACACATCTGACGCCGGAGTTATCGT10540.22636192996095578No Hit
CGCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTG10370.22271093109061782No Hit
CGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT9880.2121874637584671No Hit
GAATGATACGGCCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATG9780.21003981736415064No Hit
TTCCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCT8320.17868418000713018No Hit
TGCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTG8270.17761035680997198No Hit
TCCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTG7890.16944930051156937No Hit
GAATGATACGGCGCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTAT7430.1595701270977136No Hit
GAATGCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTT6460.13873795707284386No Hit
GAATGATACGGCGACCACCCTGTCTCTTATACACATCTGACGCCGGAGTTA5720.12284537375490201No Hit
CGTTTTTTTTCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCC5510.11833531632683741No Hit
CGTTCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTC5310.11404002353820447No Hit
TTCTGTCTCTTATACACATCTGACGCCGGAGTTATCGTATGCCGTCTTCTG5000.10738231971582342No Hit

[FAIL]Adapter Content

Adapter graph

[WARN]Kmer Content

Kmer graph

SequenceCountPValueObs/Exp MaxMax Obs/Exp Position
GATCCTC253.887218E-545.0000049
GCACCTA650.045.0000049
GCCGATG253.887218E-545.0000049
TCGCTCG253.887218E-545.0000041
GATTGTA253.887218E-545.00000420
TACCGGG253.887218E-545.0000043
GGCTAAT253.887218E-545.0000048
CTATGCG207.028958E-445.01
TCGTTAG207.028958E-445.01
CCGGGTC207.028958E-445.05
TGCCCCG207.028958E-445.01
GGTAATC406.7993824E-945.08
CCGGCAG406.7993824E-945.011
TATGGCG207.028958E-445.01
CGGTTCG207.028958E-445.033
CGCATCC207.028958E-445.045
CACGAGG207.028958E-445.015
CGATTAT207.028958E-445.010
CGTTAGG207.028958E-445.02
CTTTGCG850.045.01