Genetic Testing Solutions
Starting from Conception

We offer end-to-end sequencing solutions for newborn genetic screening and carrier screening including difficult assays such as spinal muscular atrophy (SMA) . We can also help you internalize noninvasive prenatal testing (NIPT). In addition to development of your laboratory processes, we will work to ensure that back-end analysis pipelines are properly defined and reporting solutions are completely integrated from sequencer all the way to your laboratory information system. For those laboratories who have chosen not to retain an on-site geneticist, we can provide data analysis and case review on an ad hoc or ongoing basis.