Depth of sequencing coverage of matched sample set (N = 6 unique samples).

Percent of on-target bases (y-axis) covered at a given sequence depth
(x-axis). On target percentage calculated as the fraction of nucleotide
bases falling on targeted regions divided by the total number of
nucleotides mapping anywhere in the genome. Thick lines represent
average coverage for each platform (Agilent
Surelect = blue circles; Nimblegen
SeqCap = green triangles; Raindance parallel
PCR = red diamonds). Dashed lines represent two
standard deviations above and below the average for each platform.