Skip to main content

Table 7 Running time of different methods for simulated reads with 8× coverage on chromosomes 21 and 22

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

Method

Time (s)

 
 

Minimap2

NGMLR

Find reads in fastQ

Unify outputs

SAM to BAM

Sniffles

SVIM

Remove redundancy

Total

Speed-up

Baseline method

163

–

–

–

47

27

–

–

233

0.24

NGMLR-Sniffles

–

1586

–

–

42

25

–

–

1653

1.68

Most sensitive method

163

1586

–

16

50

29

35

2

1881

1.91

SVNN

163

590

104

13

50

27

32

2

981

1