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Figure 4 | BMC Genetics

Figure 4

From: Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation

Figure 4

Results of the sequencing experiments. (A) Reads from the mRNA-seq experiment aligned across the deletion and visualised in IGV. Reads are represented by grey bars, with the deletion indicated with a black horizontal line in reads. A single nucleotide polymorphism (c.5580 T > C) is also located 18 bp downstream of the deleted sequence in the NCCD case, and is highlighted in blue. (B) Sanger sequencing to confirm the 8 bp deletion in the case, the sire of the case (obligate heterozygote) and a wild-type individual (sibling). The 8 bp sequence upstream of the deletion is identical to the deleted sequence.

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BMC Genomic Data

ISSN: 2730-6844

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