Find out how genome panels can fit into your practice

Harnessing the power of genome sequencing

Genome panels are expertly curated gene panels that use genome sequencing to offer unparalleled coverage.

This genome sequencing-based method allows clients to experience all of the traditional benefits of whole genome sequencing, including more uniform coverage in targeted genes.

  • Full intronic coverage
  • Single nucleotide variants
  • Short tandem repeat screening
  • Mean coverage 40x across introns and exons
  • Reliable detection of intragenic deletions and duplications (≥ 3 exons)

Experience unparalleled coverage


Contact PerkinElmer Genomics for more information


Why choose PerkinElmer Genomics?

• Led by world-renowned geneticists and a team of board-certified geneticists
• Over 20 years’ experience in NBS and rare disease screening with over 500M babies tested globally

Technologies & Assay Design
• Meeting or surpassing industry standards with regards to testing coverage and assay design
• Utilizing the newest in NGS technologies

• Leveraging PerkinElmer’s position as an industry-leader in NGS work-flow solutions, we create unmatched efficiency and sustainability within the lab

• Accelerating the delivery of results to clinicians and families with industry-leading TATs for panels, exomes, and genomes

Finding the Right Test
• Comprehensive and flexible testing menu to ensure that you can always find the test that best meets the patient’s needs

Sample Collection
• Multiple sample types to ensure quick and timely sample collection

Reducing Costs 
• A commitment to pass on cost savings realized through our unique automation and stream-lined processes to our clients

Overall Costs 
• Industry-leading pricing structures across testing platforms, from genome to targeted single site testing

Cost Certainty
• Transparent pricing structure based on testing platform – Panel vs. Exome vs. Genome