Information capture using SNPs from HapMap and whole-genome chips differs in a sample of inflammatory and cardiovascular gene-centric regions from genome-wide estimates

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Figure 1.
Figure 1.

Information measures for 78 genes using combined SeattleSNPs/PARC and HapMap data for extension windows of 0–200 kb around the sequenced region. Mean maximum r2, capture rates, and noncapture rates are shown by squares, circles, and triangles, respectively; European and African descent samples are distinguished by solid and open symbols, respectively.

This Article

  1. Published in Advance September 25, 2007, doi: 10.1101/gr.5996407 Genome Res. 17: 1596-1602

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