Estimating genotype error rates from high-coverage next-generation sequence data

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 4.
Figure 4.

Average number of called SNVs shared between platforms or unique to one platform (A), and the genotype discordance rate (between blood and saliva samples) for shared and platform-specific SNVs (B).

This Article

  1. Published in Advance October 10, 2014, doi: 10.1101/gr.168393.113 Genome Res. 24: 1734-1739

Preprint Server



Current Issue

  1. January 2026, 36 (1)
  1. Current Issue
  1. Alert me to new issues of Genome Research