Bloomberg the Company & Products

Bloomberg Anywhere Login


Connecting decision makers to a dynamic network of information, people and ideas, Bloomberg quickly and accurately delivers business and financial information, news and insight around the world.


Financial Products

Enterprise Products


Customer Support

  • Americas

    +1 212 318 2000

  • Europe, Middle East, & Africa

    +44 20 7330 7500

  • Asia Pacific

    +65 6212 1000


Industry Products

Media Services

Follow Us

April 01, 2015 9:29 PM ET

Healthcare Equipment and Supplies

Company Overview of Sequenom Center for Molecular Medicine, LLC

Company Overview

Sequenom Center for Molecular Medicine, LLC develops a range of molecular genetic laboratory tests with a focus on prenatal and ophthalmological diseases and conditions. The company offers MaterniT21 PLUS test for fetal aneuploidies that analyzes the relative amount of 21, 18, 13, X and Y chromosomal material in circulating cell-free DNA from a maternal blood sample; Heredi-T cystic fibrosis carrier screen test that detects a phenotypically-confirmed panel selected from the John Hopkins CFTR2 database; SensiGene fetal RHD genotyping test for the analysis of fetal RHD genotype; and RetnaGene AMD test for age-related macular degeneration. Its laboratory tests provide early patient management i...

301 Michigan Street NE

Suite 580

Grand Rapids, MI 49503

United States





Key Executives for Sequenom Center for Molecular Medicine, LLC

Chief Financial Officer
Age: 61
Vice President of National Accounts & Payor Strategies
Laboratory Director and Executive Director
Medical Director
Vice President and General Manager
Compensation as of Fiscal Year 2014.

Sequenom Center for Molecular Medicine, LLC Key Developments

Sequenom Center for Molecular Medicine, LLC Enters into Agreement for Services with Quest Diagnostics Incorporated to Provide its MaterniT21 Plus Laboratory-Developed Test Service

On June 13, 2014, Sequenom Inc., through its wholly-owned subsidiary Sequenom Center for Molecular Medicine, LLC (SCMM), entered into an agreement for services with Quest Diagnostics Incorporated, pursuant to which SCMM will provide its MaterniT21 PLUS laboratory-developed test service to Quest, and has agreed to provide a related laboratory-developed test service to Quest in the future following its commercialization (such related future test service, the Future Testing Service, and together with the MaterniT21 PLUS laboratory-developed test service, the Testing Services). After an initial period following the execution of the services agreement through the term of the services agreement, Quest has agreed not to order from or contract with any other laboratory, other than SCMM, for the provision of non-invasive prenatal testing services for or on behalf of Quest's physician customers and their patients (the Quest Exclusivity) and SCMM has agreed not to provide or contract with any third party laboratory that has securities that are traded on a public stock exchange with annual revenues greater than one billion dollars for the testing services. Notwithstanding the foregoing, in the event that the Future Testing Service is not commercialized by SCMM by a date sometime in the fourth quarter of 2014, then the Quest Exclusivity shall immediately terminate. Pursuant to the services agreement, Quest has agreed to pay SCMM a fixed fee for each Testing Service performed by SCMM on Quest's behalf. The services agreement has a term of two years, but shall automatically renew for additional terms of one year each unless either party provides at least 60 days prior written notice to the other party; provided, however, that the services agreement can be earlier terminated by the mutual agreement of the parties, by a party upon an uncured material breach of the services agreement by the other party, by Quest if any action is taken against SCMM to revoke, suspend or terminate any license to operate a clinical laboratory or to revoke, suspend or terminate SCMM’s participation in Medicaid, Medicare or other federally funded programs, and such action is not resolved within 90 days, or by Quest if the testing services are determined by a court to infringe the intellectual property of a third party and SCMM has not obtained the rights necessary to enable Quest to continue to use the testing Services or an alternative and comparable testing service.

Sequenom Center for Molecular Medicine Launches the Enhanced Sequencing Series for the MaterniT21(TM) PLUS Test

Sequenom Center for Molecular Medicine has launched the Enhanced Sequencing Series for its MaterniT21(TM) PLUS laboratory-developed test (LDT). The MaterniT21 PLUS test will begin reporting additional findings for the presence of subchromosomal microdeletions and autosomal trisomies for chromosomes 16 and 22, in addition to the previously announced additional findings for sex chromosome aneuploidies involving an abnormal number of the X or Y chromosomes. These additional findings complement the MaterniT21 PLUS test core identification of trisomies for chromosome 21, chromosome 18 and chromosome 13. With this expansion, the MaterniT21 PLUS test is the first-of-its-kind noninvasive prenatal technology (NIPT) to provide these comprehensive results from a maternal blood draw. Sequenom Laboratories will begin reporting on these select, clinically relevant microdeletions, including 22q11.2 deletion syndrome, Cri-du-chat syndrome, Prader-Willi/Angelman syndrome, 1p36 deletion syndrome, as well as trisomies 16 and 22 the last week of October. Results from a method validation study demonstrated high performance of the MaterniT21 PLUS test in accurately detecting these autosomal trisomies and select microdeletions.

Sequenom Center for Molecular Medicine, LLC and CombiMatrix Corporation Enters into Collaboration Agreement to Market Chromosomal Microarray Analysis for Prenatal Testing

Sequenom Inc. and CombiMatrix Corporation announced that the Sequenom Center for Molecular Medicine LLC (Sequenom CMM) and CombiMatrix have entered into a collaboration agreement to market chromosomal microarray analysis (CMA) testing services to broaden and confirm the results of noninvasive, prenatal testing (NIPT) to physicians and their patients. Under the agreement, the two laboratories will collaboratively use their respective marketing channels and sales forces to promote the use of NIPT and CMA and work together to provide technical training to physicians and counseling, education and support services to physicians and their patients. The two companies plan to provide, when clinically appropriate, a comprehensive test result report for ordering physicians. Sequenom is a global leader in the NIPT market, and Sequenom CMM, its wholly owned subsidiary laboratory, developed the MaterniT21(TM) PLUS laboratory-developed test (LDT), a widely-ordered, noninvasive prenatal testing service for fetal chromosomal abnormalities. CombiMatrix is one of the few independent laboratories that specialize in CMA, the primary genetic test to evaluate newborns with birth defects that is now being more widely used for prenatal testing.

Similar Private Companies By Industry

Company Name Region
ulrich medical USA, Inc. United States
Advanced Radiation Therapy, LLC United States
Oceanic Medical Products, Inc. United States
Memory Dx, LLC United States
Circadiance LLC United States

Recent Private Companies Transactions

No transactions available in the past 12 months.

Stock Quotes

Market data is delayed at least 15 minutes.

Company Lookup

Most Searched Private Companies

Company Name Geographic Region
Lawyers Committee for Civil Rights Under Law United States
Bertelsmann AG Europe
NYC2012, Inc. United States
Rush University United States
Citizens Budget Commission United States

Sponsored Financial Commentaries

Sponsored Links

Report Data Issue

To contact Sequenom Center for Molecular Medicine, LLC, please visit Company data is provided by Capital IQ. Please use this form to report any data issues.

Please enter your information in the following field(s):
Update Needed*

All data changes require verification from public sources. Please include the correct value or values and a source where we can verify.

Your requested update has been submitted

Our data partners will research the update request and update the information on this page if necessary. Research and follow-up could take several weeks. If you have questions, you can contact them at