Genomic Testing

Clinical Exome Sequencing and Whole Exome Sequencing help fill the gaps for patients whose needs go beyond preset and custom panel options. These are patient-centric, phenotype-driven analyses designed to examine coding regions and splice junctions for thousands of genes. Reports will only include the variants that are of plausible clinical relevance to your patient.

Available for testing on prenatal specimens in the case of abnormal ultrasound findings. This analysis includes DNA only. All cases subject to laboratory approval. Please contact Client Services prior to sending in the sample.