Methods & Services
We provide different DNA sequencing options to choose from. Our Sequence Analysis uses a proprietary targeted sequencing method, OS-Seq™, developed at Stanford University, to detect SNPs and small INDELs in the patient’s DNA. Alternatively, targeted Del/Dup (CNV) Analysis uncovers larger changes in the DNA. Both of these sequencing methods can be combined in our Plus Products. We also provide Whole Genome Del/Dup (CNV) Analysis to screen larger changes throughout the genome. We offer Whole Exome Sequencing as an efficient and comprehensive test where all protein-coding genes of the genome are sequenced to provide diagnoses in genetic disorders across various medical specialties.