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Table 3 Sequencing and variant calling errors of next-generation sequencing based on the data set of Sanger sequences of 13 AL8/78 BAC clones

From: Annotation-based genome-wide SNP discovery in the large and complex Aegilops tauschii genome using next-generation sequencing without a reference genome sequence

Error type

Platform

Overall error rate

INDEL error rate

Substitution error rate

Insertion (%)

Deletion (%)

Substitution (%)

Sequencing error compared with Sanger sequences

Single read error

Roche 454 GS-FLX Titanium

7.4 × 10-3

6.2 × 10-3

1.2 × 10-3

42.41

41.93

15.66

Consensus error

Roche 454 GS-FLX Titanium

1.3 × 10-3

1.0 × 10-3

3.0 × 10-4

25.20

55.56

19.24

 

Illumina Solexa

4.4 × 10-4

9.0 × 10-5

3.5 × 10-4

3.46

17.78

78.77

 

AB SOLiD v2.0

4.3 × 10-4

2.5 × 10-4

1.8 × 10-4

10.69

47.58

41.73

Variant calling errors using Roche 454 sequence as reference

Consensus error

Roche 454 GS-FLX Titanium

3.79 × 10-3

1.12 × 10-3

2.67 × 10-3

11.82

17.66

70.52

 

Illumina Solexa

1.87 × 10-3

4.1 × 10-4

1.46 × 10-3

8.41

13.7

77.87

 

AB SOLiD v2.0

5.9 × 10-4

2.7 × 10-4

3.2 × 10-4

21.71

24.67

53.62