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Figure 2 | BMC Genomics

Figure 2

From: Accurate detection of subclonal single nucleotide variants in whole genome amplified and pooled cancer samples using HaloPlex target enrichment

Figure 2

Sequence depth variation in genomic DNA (gDNA) and whole genome amplified DNA (wgaDNA) samples. Density plot showing the variation in HaloPlex sequence depth of 1509 candidate single nucleotide variants (SNVs) and 19 germline SNPs in gDNA and wgaDNA samples. The sequence depth is more uneven in the wgaDNA samples, which display relatively low or high coverage at more sites. To increase clarity, sites with a depth > 5000 are shown at 5000 and the x-axis has been cut at 0 and 5000.

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