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APF Genomics Research Services - Overview
Through the Genomics Research team at the APF, genotyping mice and fine-mapping of causal mutations is available as a fee-for-service.
In June 2011 the APN introduced a new service - a Next Generation sequencing pipeline for causal mutation identification in mouse variant strains. The service includes high throughput, mass sequencing of mouse exomes on the Illumina platform. Combined with a high quality bioinformatics capability, the APN’s Single Nucleotide Variation (SNV) detection pipeline is opening up a quantum leap in mammalian phenomics and increased access to useful mouse models of human disease.
Follow the links below to find out more about one of the many services offered by the APF Genomics Research Services:
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