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Table 1 Summary of the efficiency of our identification methods.

From: ParMap, an algorithm for the identification of small genomic insertions and deletions in nextgen sequencing data

 

Number of Genomic Variation Candidates

Number of Confirmed Candidates

Percentage

Singe-base Analysis

66

61

92%

ParMap

7

4

57%

Total

73

65

89%

  1. In total, 89% of our candidates were confirmed via Sanger sequencing.