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. 2010 Aug 25;5(8):e12397. doi: 10.1371/journal.pone.0012397

Table 2. Location of true positive variants in the genomes of mutant B. anthracis compared to the reference genome.

Strain Parent strain Start position Stop position Reference allele Sample allele Locus description Coverage % Concordance
HS-2-1 ΔANR 6,848 6,848 C T gyrA 5 100%
3,364,887 3,364,887 G A parC 5 100%
4,009,233 4,009,233 G A Stage 0 sporulation protein A 6 100%
4,373,941 4,373,941 C A Hypothetical protein GBAA4810 6 100%
HS-2-5 ΔANR 6,848 6,848 C T gyrA 10 100%
2,667,930 2,667,930 T - Hypothetical protein GBAA2880 14 100%
3,364,887 3,364,887 G T parC 9 100%
4,500,491 4,500,491 G A intergenic 9 100%
HS-2-5-6 HS-2-5 841,481 843,099 1618 bp Δ tetR family transcriptional regulator 0 (Δ)* 100%
3,588,786 3,588,786 T C phosphodiesterase 14 100%
4,009,850 4,009,873 24 bp Δ Stage 0 sporulation protein A 11 100%
4,047,733 4,047,733 G T Hypothetical protein GBAA4446 21 100%
gerH::ery ** 34F2 chr 4,524,685 4,524,685 - EryR gerHA 45 100%
2,099,226 2,099,226 T C HSP20 family protein 33 100%
pXO1 172,178 172,178 20 bp Δ none 66 95%
AP50R 34F2 chr 895,066 895,066 A - csaB 14 100%
3,894,626 3,894,626 G A 2,3-diketo-5-methylthiopentyl-1-phosphate enolase 8 100%

*coverage for the 5′ base (841,480) flanking the deletion was 13x and the 3′ base (843,100) flanking the deletion was 4x.

**includes both FLX and Titanium runs.