High-throughput discovery of rare insertions and deletions in large cohorts

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Figure 3.
Figure 3.

Comparison between SPLINTER and other variant calling algorithms: Substitutions (A,B) and indels (C,D) were analyzed independently. For each approach, performance was evaluated by assessing sensitivity (fraction of true-positive hits divided by total positives in the set) and positive predictive value (fraction of true-positive hits divided by total hits).

This Article

  1. Published in Advance November 1, 2010, doi: 10.1101/gr.109157.110 Genome Res. 20: 1711-1718

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