Figure 2From: High throughput sequencing in mice: a platform comparison identifies a preponderance of cryptic SNPsRead depth for Applied Biosystems' SOLiD (red) and Illumina's Genome Analyzer (blue) realignments. For D2 and B6 strains for the 171.6–174.6 Mb region of chromosome 1, each tick indicates the average read depth within the corresponding 25,000 bp bin.Back to article page