Genomics has ushered in a big paradigm shift in health care. This rapidly evolving field is exciting.
This exciting time also comes with some ambivalence. How does a practitioner discern what is true and what is speculation? The genome is massive. How do you even know if a SNP is actionable and well researched? Where does a practitioner start to learn the science of nutritional genomics in a non-intimidating method?
“Thank you so much for breaking down this overwhelming area of Nutritional Genomics into incremental steps rather than bombarding me with an advanced course or too much information. These incremental implementation steps are so unique.”
The field is advancing rapidly and more information is quickly becoming available.
PureGenomics is grounded in reliable science. The collective body of research on each marker is evaluated by a team of physicians, PhDs, and nutritionists to determine the strength of the evidence and whether the associated phenotype responds to nutritional or lifestyle factors. Each SNP in PureGenomics is assigned an evidence score that quantifies the level of supporting scientific evidence between the SNP and its associated effect.
PureGenomics has simplified all the noise in the industry into a concise, easy to read report that makes genetics simplified. No longer do you have to be an expert in genetics to understand how to include this tool in your toolbox.
The time to integrate this clinical decision-making tool into your practice is now, and the PureGenomics platform makes it easy to get started.