FastQCFastQC Report
Mon 3 Dec 2018
G166_M12.R2.fastq

Summary

[OK]Basic Statistics

MeasureValue
FilenameG166_M12.R2.fastq
File typeConventional base calls
EncodingSanger / Illumina 1.9
Total Sequences34011303
Sequences flagged as poor quality0
Sequence length50
%GC69

[OK]Per base sequence quality

Per base quality graph

[OK]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

[FAIL]Sequence Duplication Levels

Duplication level graph

[FAIL]Overrepresented sequences

SequenceCountPercentagePossible Source
GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG449462413.215089113169231No Hit
CGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGACTGGAGTTCAGACGTGTG4769191.4022367799316597Illumina Single End PCR Primer 1 (96% over 32bp)
CGCGTCACCCGCTGCGGTGGGTGCTGCGCGGCTGGGAGTTTGCTCGCAGG1078920.3172239534604129No Hit
GACGATCAATCGCGTCACCCGCTGCGGTGGGTGCTGCGCGGCTGGGAGTT994190.2923116471015533No Hit
GGGAACCCACCGCGCCCCCGTGGCGCCCGGGGGTGGGCGCGTCCGCATCT755390.22209969432808851No Hit
GTCACCCCATTGATCGCCAGGGTTGATTCGGCTGATCTGGCTGGCTAGGC660930.19432657431560327No Hit
CGGGATTTGTGCCGGGGACGGAGGGGAGAGCGGGTAAGAGAGGTGTCGGA632900.18608519644190052No Hit
CCCAACCCGGGTCGGGCCCTCCGTCTCCCGAAGTTCAGACGTGTGGGCGG598040.1758356626325078No Hit
TCAGACGTGTGGGCGGTTGTCGGTGTGGCGCGCGCGCCCCGCGTCGCGTG586790.1725279387267227No Hit
GTCGGTGTGGCGCGCGCGCCCCGCGTCGCGTGAGCCTGGTCTCCCCCGCG540250.15884425245336822No Hit
GGCGCCCGGGGGTGGGCGCGTCCGCATCTGCTCTGGTCGAGGTTGGCGGT524250.15413993400958498No Hit
GCGTCACCCGCTGCGGTGGGTGCTGCGCGGCTGGGAGTTTGCTCGCAGGG471330.13858040075677194No Hit
CCGTCTCCCGAAGTTCAGACGTGTGGGCGGTTGTCGGTGTGGCGCGCGCG452460.13303224519213508No Hit
TGACGATCAATCGCGTCACCCGCTGCGGTGGGTGCTGCGCGGCTGGGAGT426360.1253583257307137No Hit
GCCAACCCACCGCCCTGTGCTCCGCGCCCGGTGCGGTCGACGTTCCGGCT407470.11980428976802213No Hit
TTTGACCCGTCCCGGGGGCGTTCGGTCGTCGGGGCGCGCGCTTTGCTCTC406400.11948968847209412No Hit
TTGGGTCTTGCGCTGGGGGAGGCGGGGTCGACCGCTCGCGGGGTTGGCGC400350.11771086806053857No Hit
GGCGGTTGAGGGTGTGCGTGCGCCGAGGTGGTGGTCGGTCCCCTGCGGCC396990.11672296118734411No Hit
GGGGACGGAGGGGAGAGCGGGTAAGAGAGGTGTCGGAGAGCTGTCCCGGG396550.11659359243014007No Hit
GTGATTCCCGCCGGTTTTGCCTCGCGTGCCCTGACCGGTCCGACGCCCGA387300.11387390832982788No Hit
TCCACCGTGGCGGTGCGCCGCGACCGGCTCCGGGACGGCCGGGAAGGCCC373010.10967236391972399No Hit
TGGGTCTTGCGCTGGGGGAGGCGGGGTCGACCGCTCGCGGGGTTGGCGCG364250.10709674957175266No Hit
GCTGCGCGGCTGGGAGTTTGCTCGCAGGGCCAACCCCCCAACCCGGGTCG346790.1019631620699742No Hit
GCCGCCCGAGTTCACGGTGGGTTCGTCCTCCGCCTCCGCTTCTCGCCGGG340460.10010201608565247No Hit

[OK]Adapter Content

Adapter graph

[FAIL]Kmer Content

Kmer graph

SequenceCountPValueObs/Exp MaxMax Obs/Exp Position
TAGACTG729950.038.51648329
AGACTGG750500.037.26554530
GTAGACT769300.037.21836528
GACTGGA747800.037.05911331
TGTAGAC893900.036.27583327
ACTGGAG766350.036.19083432
CTGGAGT766600.036.05817433
TGGAGTT808500.035.473934
GGAGTTC918250.034.2218235
TAGACGG26600.033.49517429
GATCGGA440450.033.1380771
AGTGTAG1079850.032.7998125
GTGTAGA1089750.032.46549626
ATCGGAA458000.032.2185132
TCGGAAG467300.032.0198333
GAGTGTA1157350.031.20789124
ATCATCG38300.030.789932
AGAGTGT1208150.030.6622723
TCATCGA38800.030.5065173
AAGAGTG1221150.030.47276522