space
Strengthening the bonds
that matter most
Building the framework to re-define pediatric diagnostics
through integrated partnerships learn more
family in field of grass
Answers in Weeks,
Not Years
Discover the power of the orthogonal approach
and the CLARITAS Experience learn more
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CLARITAS = ANSWERS
Learn how the CLARITAS Experience brought Jackie's
32 year diagnostic odyssey to an end learn more
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Fast. Confirmed.
Focused.
Claritas Clinical Exome: Orthogonally-confirmed,
clinically-relevant results within 12 weeks learn more
  • November 27, 2017

    Claritas Genomics has launched the new and improved high resolution deletion/duplication array for its Claritas Clinical Exome (CCE) and Region of Interest (ROI) tests. It can be ordered as a standalone array or as a companion to the CCE and ROIs. The new high resolution array contains 800K probes for CNVs and 100K SNPs. More information can be found here.

  • November 21, 2017

    Claritas Genomics is pleased to announce the Severe Combined Immunodeficiency (SCID) Region of Interest assay, which was developed in collaboration with leading experts in pediatric immunology and evaluates 59 genes related to known causes of SCID. More information on the assay can be found here....

  • November 07, 2017

    Claritas will be exhibiting at the 2017 Labroots Clinical Diagnostics & Research virtual event on November 8th and 9th. Visit the website to learn more about the event. Register here.

About Claritas

Claritas Genomics serves children affected with complex genetic disorders by providing timely and accurate results, resolving families’ long search for answers. By combining clinical expertise of the world’s best pediatric specialists with innovative platform solutions, Claritas is working to improve patient care and enable new discoveries. We are committed to the highest quality and accessibility of information and our interpretive services and unique approach to reporting set the standard for reliably and clearly communicating genetic information.

Now is the time to integrate genomics into clinical practice to inform, guide and improve medical treatment for kids around the world.