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

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Figure 2.
Figure 2.

Average number of SNVs called per sample, stratified by GQ score (x-axis) and average level of coverage. Each “lane” corresponds to 32 GB of total sequence.

This Article

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

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