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Table 3 SNP content of the major nodes identified in the phylogenetic tree (cladogram)

From: Whole genome single nucleotide polymorphism based phylogeny of Francisella tularensis and its application to the development of a strain typing assay

Node

Sub-species/clade/sub-clade

Number of strains per node

Total SNPs

Total SNPs in LVS genome

Total SNPs in SchuS4 unique sequence

Common SNPs

Unique SNPs

Differentiating SNPs

Maximum SNP separation

50

B

13

3771

3686

85

5

2837

3656

2833

51

B*

12

1154

1115

39

6

233

1060

602

52

B1

7

779

750

29

385

164

161

76

64

B2

5

705

677

28

7

153

628

549

4

A

26

8653

8559

94

2905

514

3765

2779

39

A2

6

6003

5919

84

3789

358

316

201

5

A1

20

7306

7291

15

4953

323

497

176

8

A1a

9

7001

6993

8

5491

277

129

75

23

A1b

10

7030

7022

8

5537

234

71

38

  1. * contains all the type B strains with the exception of FRAN024, Japanese holarctica strain.
  2. Total SNPs are locations at which a SNP occurs in one or more strains in the node (if the same SNP occurs in more than one strain, that location is counted only once). Common SNPs are locations where all strains in the node share the same base call, which is different from the reference call on the resequencing platform. Unique SNPs are locations where just a single strain in the node has a base call that differs from the reference sequence. Differentiating SNPs are locations at which at least two strains in the node have different base calls. Maximum SNP separation is the number of base calls separating the two most distant members of the node. Differentiating SNPs and maximum SNP separation are both indicators of the degree of diversity within the node. The detection of diversity is limited by the extent to which our sample set is representative of the variability within each clade in nature. Refer to Figure 2 for the details of strain clustering.