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Table 3 Genome assembly continuity and correctness comparison to secondary technologies

From: Reducing assembly complexity of microbial genomes with single-molecule sequencing

Organism

Assembled with

Assembly bp

Contigs

N50

LAP

Discordant bases

QV

E. coli K12

MiSeq 100× 2×150 bp 300 bp (MaSuRCA iCORN)

4,682,345

139

113,852

-9.68E + 07

28

52.23

 

454 50×

4,569,757

93

117,490

-9.73E + 07

17

54.29

 

PBcR 200×

4,653,486

1

4,653,486

-9.64E + 07

3

>60

E .coli O157:H7

MiSeq 100× 2×150 bp 500 bp (SPAdes iCORN)

5,433,737

413

133,641

-3.67E + 07

62

49.43

 

454 22× + 8× 5 kbp + 10× 10 kbp

5,347,050

409

133,665

-3.73E + 07

66

49.09

 

PBcR 200×

5,611,389

9

4,324,437

-3.66E + 07

0

>60

B. trehalosi

MiSeq 100× 2×150 bp 500 bp (SPAdes iCORN)

2,377,594

83

222,446

-3.31E + 07

10

53.76

 

454 50×

2,364,704

66

117,742

-3.32E + 07

9

54.20

 

PBcR 200×

2,411,068

1

2,411,068

-3.27E + 07

0

>60

M. haemolytica

MiSeq 100× 2×150 bp 500 bp (MaSuRCA iCORN)

2,721,965

89

84,094

-3.33E + 07

47

47.63

 

PBcR 200×

2,736,037

1

2,736,037

-3.31E + 07

0

>60

F. tularensis

MiSeq 100× 2×250 bp 500 bp (SPAdes iCORN)

1,825,374

130

24,065

-1.33E + 07

0

>60

 

454 50×

1,655,657

326

7,316

-1.33E + 07

28

47.72

 

PBcR 300×

1,877,407

3

573,021

-1.33E + 07

0

>60

S. enterica Newport

MiSeq 56× 2×150 bp 500 bp (MaSuRCA iCORN)

5,187,269

114

195,780

-2.24E + 07

360

41.59

 

454 23× + 2× 10 kbp

5,005,089

172

372,513

-2.25E + 07

39

51.08

 

PBcR 200×

5,029,197

2

4,919,684

-2.24E + 07

2

>60

  1. Organism: the genome being assembled. Assembled with: the sequencing data used for assembly. 454 sequencing was unpaired FLX+, with paired-end sequencing available for some genomes, as indicated. MiSeq sequencing was paired-end, indicated as 2×Xbp Yb where X is the target read length and Y is the paired-end size. Column definitions are the same as in Table 2. PacBio RS sequences were self-corrected and assembled as in Table 2. 454 sequences were assembled with Newbler [39] and MiSeq sequences were assembled with SPAdes [43] and MaSuRCA [38, 44]. Both assemblies were polished using iCORN [45] and the one with the best LAP score was reported.