Using an integrated omics-based approach, PerkinElmer Genomics is a global leader in genetic and genomic testing focused on rare diseases, hereditary cancer, inherited conditions, and newborn screening. Our services support the full continuum of care from preconception and prenatal to neonatal, pediatric, and adult. Testing options include sequencing for targeted genes, multiple genes, the whole exome or genome, and copy number variations. Using a simple saliva or blood sample – including dried blood spot, we answer complex genetic questions that can proactively inform patient care and end the diagnostic odyssey for families.