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Complex disease and phenotype mapping in the domestic dog
Jessica J Hayward1, Marta G Castelhano2, Kyle C Oliveira1
1Department of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853, USA.
Nature Communications
|January 23, 2016
Summary
This study used the largest canine genome-wide association study to date to identify genetic loci for complex diseases like hip dysplasia and cancer in dogs. Findings will accelerate genetic research for canine and human diseases.
Area of Science:
- Veterinary genetics
- Comparative genomics
- Medical genetics
Background:
- The domestic dog is a valuable model organism in medical genetics.
- Canine studies offer insights into human diseases, including cancer and orthopaedic conditions.
Purpose of the Study:
- To conduct the largest canine genome-wide association study (GWAS) to date.
- To accelerate the identification of genetic loci associated with complex canine diseases and morphological traits.
Main Methods:
- Genotyping over 4,200 dogs at 180,000 markers.
- Performing genome-wide association studies for complex diseases and quantitative traits.
Main Results:
- Identified significant loci associated with hip dysplasia, elbow dysplasia, idiopathic epilepsy, lymphoma, mast cell tumor, and granulomatous colitis.
- Reported three novel quantitative trait loci influencing body size and one influencing fur length and shedding.
- Simulation studies indicate that larger sample sizes and denser marker sets can identify most moderate- to large-effect complex disease loci.
Conclusions:
- The study provides a framework for efficient genetic mapping of canine complex diseases.
- Canine genetic studies can be achieved with fewer samples than human studies, given appropriate design.
- Findings advance understanding of canine genetics and have implications for human disease research due to shared genetic architecture.
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