Genomic Sequencing (NGS)
Multi-gene tests that detect both known and unknown disease-causing mutations.
Genomic Sequencing
Using next-generation sequencing (NGS), our hereditary screening tests can detect mutations in a person’s genes that are known to cause certain cancers, cardiomyopathy, and pulmonary disease. We also offer whole genome and whole exome screening, when a specific genetic cause is uncertain, and sequencing of positive SARS-CoV-2 samples for variant identification.
Genetic Counseling
Genetic counseling aids individuals and families in comprehending the implications of genetic information. Our dedicated team provides insights into potential genetic risks, guidance on testing options, and support to make informed decisions. Explore our Test Menu for more comprehensive offerings.
The AlphaDERA Difference
At Alphadera Labs, we're redefining genetic testing. Through advanced precision and clarity, we offer both healthcare professionals and individuals a deep dive into the genetic blueprint. Our commitment goes beyond mere results; it's about providing actionable insights and fostering a deeper understanding of oneself. Together, we're ushering in a new era where science meets personalized care, ensuring every test is a step towards a healthier, informed future.
Contact Us
