An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

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Figure 7.
Figure 7.

Nonreference genotype concordance for low-pass genome data calculated using Omni2.5 array genotypes. The haplotype-aware refinement steps significantly improve genotype accuracy, especially with larger sample sizes.

This Article

  1. Published in Advance April 16, 2015, doi: 10.1101/gr.176552.114 Genome Res. 25: 918-925

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