The era of precision healthcare is here, and we are proudly at the forefront providing both Clinical reporting and Laboratory services. The role of genetics in healthcare is changing profoundly, delivering clinically actionable information, this evidence-based approach has revolutionized healthcare. With the advancement in technology, sequencing an individual’s genome is now affordable and results are provided in reasonable time frames, allowing better advice, sooner.
Our reporting services are provided by myDNA and our Laboratory Services are delivered by Gene by Gene. We are one company, which has significant advantages in providing end to end services and rapid turnaround times.
myDNA Clinical Reporting
The myDNA report is easy to understand and interpret. Doctors are presented with a summary of genetic findings related to preventative health screening. This allows doctors to provide precision medicine and Care Management Plans specifically for each patient.
Leaders in genetic data
analysis and reporting.
World class, easy to
understand reporting
Experienced
Clinical Team
Gene by Gene Laboratory Services
Gene by Gene is our leading state-of-the-art laboratory, based in Houston, Texas, USA. With over 20 years of experience analyzing genetic data, we have genetic testing requirements covered. Our advancements in technology are providing high quality, accurate testing. Our highly qualified team of experts use the most up to date research. We use highly advanced, cutting-edge genomic infrastructure to process and translate genomic data to analyze and curate accurate insights.
Rapid turnaround time
to meet your clinical needs
State of the art infrastructure
offering competitive pricing
Stringent quality control to
ensure highest quality test results
What Panels we Cover
To explore further, please see categories below for more details.
Cardiovascular Diseases
(174 Genes)
Aortic, aneurysm, familial thoracic
Arrhythmogenic right ventricular cardiomyopathy Brugada syndrome
Catecholaminergic polymorphic ventricular tachycardia
Dilated cardiomyopathy
Ehlers-Danlos syndrome, type 4
Fabry’s disease
Familial hypercholesterolemia
Familial hypertrophic cardiomyopathy
Left ventricular noncompaction
Loeys-Dietz syndrome
Long QT syndrome
Marfan’s syndrome
Tryptase
Comprehensive Health
(92 Genes)
Comprehensive Health Test
Parkinson Alzheimer and Dementia
(47 Genes)
Hereditary Cancers
(113 Genes)
Adenomatous Polyposis Coli
Birt Hogg Dube syndrome
Breast Cancer
Colorectal Cancer
Endometrial Cancer
Gastric Cancer
Gastrontestinal Stromal Tumor – GIST
Hemangi oblastomas
Juvenile Polyposis syndrome
Li-Fraumeni syndrome
Lynch syndrome
Melanoma
Multiple endocrine neoplasia
Neurofibromas
Ovarian Cancer
Pancreatic Cancer
Paragangliomas
Peutz-Jeghers syndrome
Pheochromocytomas
Prostate Cancer
PTEN hamartoma tumor syndrome
Renal Cancer
Retinoblastoma
Thyroid Cancer
Tuberous sclerosis
Von Hippel-Lindau syndrome
Diabetes, Obesity, Metabolic
(34 Genes)
Diabetes
Malignant hyperthermia
Obesity
Ornithine carbamoyltransferase deficiency
Wilson disease
Eye/Hearing
(Eye – 608 Genes) (Hearing – 146 Genes)
Eye disorder, hereditary, adult onset
Hearing loss, hereditary, adult onset
Pharmacogenomics
(26 Genes)
Psychotropic Test | Over 40 medications
Multiple Category Test | Approx. 150 medications
MTHFR
Immunodeficiency
(50 Genes)
Custom Panels
Custom reports are also available upon request. Inquire with our sales team for more information.
CAP Accredited
CLIA Accredited
AABB Accredited
CDPH Licensed
NYS DoH Authorized