Figure 6.

Screen capture for whole genome sequencing read depth and read alignments using Integrated Genome Viewer (IGV) for the five affected individuals of family A centered at genome position chr2:179,118,837 (red/blue). Read depths (lines) are scaled in a range of 0–200 for all five individuals. Red cross-lines denote variant reads; the rare variant is present in some but not all reads, indicating heterozygosity.

Toro et al. BMC Neurology 2013 13:29   doi:10.1186/1471-2377-13-29
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