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Table 2 Validation of polymorphism predictions in Est-1

From: Simultaneous alignment of short reads against multiple genomes

   

Graph analysis

Single-reference analysis

  

N a

Recallb

FDRc

Recallb

FDR

SNPs

 

2,316

85.2%

0.4%

77.5%

0.4%

Deletions

All

183

53.6%

2.0%

38.8%

2.7%

 

   1-3 bp

132

68.2%

2.2%

53.8%

2.7%

 

   ≥ 4 bp

51

15.7%

0.0

0

n/a

Insertions

All

167

53.9%

2.2%

45.5%

1.3%

 

   1-3 bp

128

66.4%

2.3%

59.4%

1.3%

 

   ≥ 4 bp

39

12.8%

0.0

0

n/a

  1. aNumber of known variants in 600 kb of dideoxy sequence data from [38]. bRatio of confirmed to the sum of confirmed and missed predictions of the respective kind; indicates sensitivity of method. cFalse discovery rate, percentage of erroneous calls.