November 16, 2015

Article initially published on STAT News
By Melissa Bailey
Guo Family
Five-year-old LamLam Guo has spent most of his life in hospitals. Since he was a baby, he has suffered from weak muscles and has had trouble eating, but doctors can’t explain why. He lies in a hospital bed in Hong Kong, wrapped in a blanket, unable to move his eyes or to breathe on his own.

His story, spread widely on Chinese social media, has caught the...

October 07, 2015

Boston, Massachusetts | October 7, 2015 – Claritas Genomics, Inc., will have six presentations at the American Society of Human Genetics (ASHG) running 10/6 – 10/10 in Baltimore, MD.  Claritas colleagues and collaborators from Boston Children’s Hospital and The Congenital Muscle Disease International Registry (CMDIR) will present data on the company’s innovative approach to deliver fast, rapidly confirmed, and phenotypically focused testing, demonstrating the benefits for patients, healthcare providers, and hospital systems.   

“So many rare childhood...

October 07, 2015

Claritas Exome-Based Tests Simplify Use of Exomes in the Clinic to Guide Precision Care for Kids

BOSTON, Massachusetts | October 7, 2015 –Today, Claritas Genomics, Inc., announced the launch of its Claritas Clinical Exome, at the Annual Meeting of the American Society of Human Genetics running 10/6 – 10/10 in Baltimore, MD. This novel diagnostic test is the first to exploit the strengths of multiple DNA sequencing platforms simultaneously to deliver confirmed results for a patient’s clinical whole exome within 4 weeks, compared to the industry...

June 23, 2015

BOSTON, Massachusetts — Today Claritas Genomics and Genetic Alliance announced a partnership to help patients and families find and participate in relevant research opportunities that will advance understanding of individual genetic disorders and development of new therapies. In this partnership, Claritas, in collaboration with patient advocacy organizations, will use the Platform for Engaging Everyone Responsibly (PEER), created by the Genetic Alliance and Private Access, to connect the patient’s genetic test and exome results to their clinical information and enable families to...

March 24, 2015

CAMBRIDGE, MA /PRNewswire-USNewswire/ — Claritas Genomics will present data on the quality of parallel multi-technology sequencing, a comparison of the company’s phenotypically driven Pediatric Neurology Exome Assay to whole exome and panel-based approaches, three-part reports for rapid results reporting, and the clinical utility of the Neurology Exome’s tailored approach compared to other tests currently on the market.

“Gene testing is transitioning from a pick and choose artisanal approach for test selection, gene selection, variant analysis and reporting, to standardized and...

January 26, 2015

Begins 2015 with $15 Million Investment by NextCODE Health (now part of WuXi-NextCODE Genomics), Boston Children’s Hospital, Cerner Corporation and Cincinnati Children’s Hospital Medical Center

CAMBRIDGE, MA – Claritas Genomics announced today that it has secured $15 million in capital for its Series B round to expand its commercial operations, launch new next generation sequencing-based tests for diagnosis of pediatric genetic disorders and continue to build its network of clinical pediatric disease...

December 14, 2014

To rapidly expand the use and power of genomic sequencing for diagnosing and treating rare diseases, Claritas Genomics and NextCODE Health today announced a strategic partnership bringing together global leadership in pediatric medicine and sequence analysis. Claritas Genomics, affiliated with Boston Children’s Hospital, is a CLIA-certified clinical laboratory serving the DNA-based diagnostic testing needs of children’s hospitals that admit hundreds of thousands of patients with genetic disorders every year. NextCODE’s solutions have been developed and proven on the world’s largest...

July 31, 2014

Claritas Genomics, a clinical laboratory serving the DNA-based diagnostic testing needs of children’s hospitals, announced today that it is launching a novel series of clinical assays that combine the flexibility and comprehensiveness of whole exome sequencing with the rigor of deep and focused analysis of variants associated with specific clinical presentations.

The first of these tests, the Claritas Pediatric Neurology Exome is a comprehensive clinical whole exome assay that is tailored to address diagnosis of...

July 24, 2014

Dr. Yiping Shen, a Clinical Genetics Medical Director at Claritas Genomics presented a webinar sponsored by Agilent Technologies on Claritas’s ClariView Array, a microarray designed for patients with autism, developmental delay, or intellectual disability.

More information about the webinar can be found by visiting Agilent’s website.

Visit the ClariView Array webpage to learn more about the microarray....

June 24, 2014

Elizabeth Boudreau, Claritas’s Senior Manager of Information Technology, was invited by Amazon Web Services to speak at the June conference in Washington, DC. The conference, “AWS Government, Education, and Nonprofits Symposium,” invited leaders in public sectors to learn more about how the AWS cloud can support their work. Ms. Boudreau’s presentation, entitled “Enhancing Genetic Computation with AWS” narrated Claritas’s history of using AWS, discussed the challenges and advantages of AWS, and outlined the business impact in using cloud-based computation. More information on the conference...

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.