PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data

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Table 1.

Heterozygous indel detection sensitivity (%) and specificity (%) of PolyScan v2.0, Mutation Surveyor v3.0, and PolyPhred v6.0b run under various parameters on the NPM1 data set

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Table 1.

In this analysis, predicted indel sites are required to be within 5 bp of the target sites to be counted as correct.

This Article

  1. Genome Res. 17: 659-666

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