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Updated: Nov 3, 2025

Novel Sequence Discovery by Subtractive Genomics
Published on: January 25, 2019
Dog10K_Boxer_Tasha_1.0: A Long-Read Assembly of the Dog Reference Genome
Vidhya Jagannathan1, Christophe Hitte2, Jeffrey M Kidd3,4
1Vetsuisse Faculty, Institute of Genetics, University of Bern, 3001 Bern, Switzerland.
Abstract:
The domestic dog has evolved to be an important biomedical model for studies regarding the genetic basis of disease, morphology and behavior. Genetic studies in the dog have relied on a draft reference genome of a purebred female boxer dog named "Tasha" initially published in 2005. Derived from a Sanger whole genome shotgun sequencing approach coupled with limited clone-based sequencing, the initial assembly and subsequent updates have served as the predominant resource for canine genetics for 15 years. While the initial assembly produced a good-quality draft, as with all assemblies produced at the time, it contained gaps, assembly errors and missing sequences, particularly in GC-rich regions, which are found at many promoters and in the first exons of protein-coding genes. Here, we present Dog10K_Boxer_Tasha_1.0, an improved chromosome-level highly contiguous genome assembly of Tasha created with long-read technologies that increases sequence contiguity >100-fold, closes >23,000 gaps of the CanFam3.1 reference assembly and improves gene annotation by identifying >1200 new protein-coding transcripts. The assembly and annotation are available at NCBI under the accession GCF_000002285.5.
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