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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.