Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

(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 5.
Figure 5.

Genotype sensitivity with increasing sequence data. Percentage of genotypes assigned in the ROI (same for all methods) with increasing filtered sequence data for NA18507 and NA12878. Sequence counts are based on 36 bases per read for MIP and SHS. To account for the 6-base index bar code, 42 bases were used in the sequence count calculations for MGS. The dashed arrow indicates genotype sensitivity level (67.3%) of 30-fold coverage whole-genome shotgun (WG) data for the ROI analyzed in this study.

This Article

  1. Genome Res. 20: 1420-1431

Preprint Server