Validation of identified variants, which were observed in only one of the DNA samples. Each set of sequence chromatograms represents a different variant that was examined by Sanger sequencing. For each, the top panel is the sample with the SNP (highlighted with the red arrow), and the bottom is the corresponding sample with the non-variant allele. Below each chromatogram are the gene, putative amino acid change, and chromosome and bp location on the chromosome.
Londin et al. BMC Genomics 2011 12:464 doi:10.1186/1471-2164-12-464