The world’s most comprehensive DNA analysis.

We offer two different service options for consumers: KnomeCOMPLETE™ results in the identification of nearly all of the roughly six billion base pairs that comprise the human genome and KnomeSELECT™ results in the sequencing of the 20,000 genes in your genome, This enables our scientists to craft a comprehensive analysis tailored specifically to each individual. GeneReviews™ are detailed reports that describe the genetic basis of specific health conditions or traits, and map the known gene-to-disease associations onto your personal DNA sequence. Because we are working with your sequence information, we can analyze all sources of genetic variation in your DNA, including common variants, rare variants and genetic changes that may be unique to only you.

Each report describes a specific condition, discusses the current standard of care for screening and prevention, and highlights the genetic basis of the condition. A summary of all variants analyzed in your personal DNA is also included. Where relevant, GeneReviews contain a summary of risk based on an analysis of the most informative genetic variants based on current research.

We create personalized GeneReviews for over 1,500 genes and over 400 conditions. Additionally, we conduct carrier screening for rare genetic disorders and generate a pharmacogenomic profile to determine how your individual genetic make-up might influence your response to specific therapeutic agents. We also create customized reports for specific traits and conditions at the request of our clients.