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Bring value to your upcoming research projects with the Prenetics Exome Sequencing service.
Prenetics are proud to offer exome sequencing, allowing us to measure 31 million positions in DNA
The exome is estimated to encompass approximately 1% of the genome, yet contains approximately 85% of disease-causing mutations. Most of our knowledge about DNA is contained within this 1%, making exome sequencing affordable, accessible and highly effective.
A clinical grade service delivered at consumer grade pricing, we are able to uniquely customise our exome sequencing service to support all consumer health, medical and research needs.
All this can be delivered at the most competitive price on the market.
The unique benefit of our exome sequencing is that it can measure for, not only Polygenic diseases, but also Monogenic diseases, allowing us to measure for 69 major diseases, 36 hereditary cancers and 163 carrier screen diseases.
Access our raw data
Access 150 features and analysis that we can provide
Use our own bioinformatics team to narrow down information
Learn about the science and discover how our exome sequencing service can help you.
Inside the pack you’ll learn: