Our services support a wide variety of research outcomes.
The way by which genes interact with one another can sometimes predispose us to developing particular diseases or alter the effectiveness of medicines and treatments.
Testing for variations in genes has become an area of great interest for researchers and practitioners hoping to develop personalized medicine treatment.
Genomics is revealing the underlying mechanisms of cancer, uncovering new therapeutic targets, and providing personalized diagnoses. Whole genome sequencing has also enabled the rapid identification and ongoing surveillance of antibiotic resistance and virulence of infectious diseases.
We offer a range of advanced genomic tools, including high-throughput genotyping, genome, transcriptome or methylome sequencing to help drive this research.
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