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Opt in to share your genetic information with our researchers
With the completion of the human genome project and recent advances in genomic science, entire human genomes can now be sequenced quickly and easily. Over 12 million genetic variants have been identified to date.
While some genetic variants are known to be pathogenic and cause disease, the clinical significance of the majority of variants discovered are still unknown.
Our laboratory is at the forefront of precision medicine, designing advanced targeted DNA test panels for diagnosing multifactorial and complex genetic diseases.