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Table 8 Running time of different methods for simulated reads with 12× coverage on chromosomes 21 and 22

From: SVNN: an efficient PacBio-specific pipeline for structural variations calling using neural networks

 

Time (s)

 

Method

Minimap2

NGMLR

Find reads in fastQ

Unify outputs

SAM to BAM

Sniffles

SVIM

Remove redundancy

Total

Speed-up

Baseline method

281

–

–

–

78

72

–

–

431

0.28

NGMLR-Sniffles

–

2687

–

–

66

67

–

–

2820

1.84

Most sensitive method

281

2687

–

51

119

77

51

2

3266

2.14

SVNN

281

766

196

43

117

74

50

2

1529

1