Research Experience

Research Sequencing

Claritas Genomics was founded to assemble and provide the basic tools and methods to obtain answers quickly and efficiently. We partner with researchers and provide access to our sequencing tools, thereby facilitating the investigation of genetic and genomic disease that can lead to answers for patients and their families.

By partnering with Claritas Genomics, you leverage our unified approach to pediatric genetics, which enables the integration of genomic information in everyday patient care and accelerates research discoveries.

Low-cost, rapid exome sequencing

Claritas offers whole exome sequencing on DNA samples for non-clinical purposes for researchers whose projects require low-cost, high-quality rapid exome sequencing.

Product specifications

1. Can accept small and large projects (1-10,000+)
2. Both Illumina and Life machines are available
3. Standard turn-around time: 4-6 weeks for 96 samples
4. A minimum of 80% of target bases covered to at least 20x depth
5. Data is processed into several output files and distributed through the Claritas-WuXi NextCODE instance.

How to order

Contact us at ResearchSequencing@claritasgenomics.com or Toll-free 855-373-9003 to discuss your project.