Make Personalized Medicine a Reality

The potential of the human genome remains unrealized for patient care. Unlock it with Clinical Genomics as a Service, a simplified platform for integrating genomics into provider practices and organizations across specialties, geographies, and sizes.

Elevate your Practice

Boost patient experience and improve clinical outcomes while capturing significant value through insourced or outsourced genetic testing.

Seamless Integration of Clinical Genomics

We provide the back-end infrastructure for practices to efficiently integrate clinical genomics into routine care. We manage the complexities of clinical-grade testing, enabling you to differentiate and personalize your care model, improve patient retention and satisfaction, and implement a sustainable new service line.

Benefit from our Scientific & Clinical Expertise

  • R&D and clinical product development
  • Bioinformatics
  • Software engineering
  • Regulatory & compliance
  • CLIA accreditation and CAP certification

Capitalize on a Simple Startup

  • Affordable startup costs
  • Simple implementation
  • Training
  • Validation
  • SOPs

Create Patient & Practice Value

  • Clinical
  • Financial

Genetics in Everyday Practice

The Clinical Necessity of Genomics

Genetic testing should be a key component of patient care, regardless of the patient’s family history or current presentation of disease.

1 in 8 cancer patients have a germline genetic variant that can be identified by genetic testing.

— Samadder NJ, Riegert-Johnson D, Boardman L, et al. Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome. JAMA Oncol. Published online October 30, 2020. doi:10.1001/jamaoncol.2020.6252

Why Genetics?

80% of rare diseases have a genetic component.

— Rare disease genomics. Genomics England Limited. Accessed online February 18, 2021. https://www.genomicsengland.co.uk/understanding-genomics/rare-disease-genomics/

Lack of access to genetic services is one of the most significant impediments to PCPs integrating genetics into their practices.

— Mikat-Stevens, N., Larson, I. & Tarini, B. Primary-care providers’ perceived barriers to integration of genetics services: a systematic review of the literature. Genet Med 17, 169–176 (2015). https://doi.org/10.1038/gim.2014.101

How Partnership Works

Managed Lab

Increase your practice’s value by internalizing genetic testing.
We establish and help operate your in-house laboratory.

Components

  • Build out the lab and support instrumentation.
  • Support staffing, training, and regulatory work.
  • Provide ongoing support and quality control.

Learn More about our Managed Lab Offering

Who is this for

  • A high-volume practice, group, or system with a well-known brand and reputation, and desire to capitalize on the opportunity for a new revenue stream and improve patient experience.

Private Labeling

Improve the patient experience with on-brand touchpoints.

Components

  • Offer your patients select next-generation sequencing (NGS) tests under your own brand.

Who is this for

  • A mid-volume practice, group, or system with a growing brand and reputation, and a desire to enrich their service offering with genetic testing.

Outsourcing

Elevate patient care with turnkey clinical-grade testing.

Components

  • Offer our at-home or in-office tests to your patients directly that retain the Phosphorus brand.

Who is this for

  • A low-volume practice that does not have or need a brand identity, but with a desire to enhance patient care with a new service offering.
Get in touch and learn which option makes the most sense for your practice.

Our Technology

Enabled by the Most Advanced Science and Technology

We leverage next-generation sequencing (NGS) and RT-qPCR testing in our state-of-the-art, CLIA-licensed, CAP-accredited laboratory. Our proprietary, end-to-end, lab operating system, Elements, integrates with practice management tools and allows for seamless flow of information between our lab and your practice.

Our Technology

The Benefits of our Tests

Help Your Patients See the Full Picture

Streamlined genetic testing at the point of care benefits patients and practices.

Clinical Grade

Our clinical grade tests are built upon expert-curated panels, powerful data analytics, a simple testing workflow, and a rigorous variant interpretation process that ensures the most accurate results for patients.

Ease of Use

Patient-friendly, flexible specimen collection methods include: a saliva kit for at-home collection, or routine venipuncture in your facility.

Counseling

Our workflow solutions can include access to genetic counselors who can interpret test results for patients and assist physicians in treatment planning.

Physician-Mediated Testing Options

Accessible Genetic Testing for Patients

PhosphorusONE

The PhosphorusONE test is the most comprehensive assessment of genetic health meant for identifying and stratifying risk for genetic conditions. The health screen analyzes 375 genes covering 170 inherited conditions and 175 different drug reactions.

Panels for specific diseases and conditions:

  • Fertility
  • Oncology
  • Neurology
  • Drug response
  • Metabolic
  • Lipidology/emias
  • Vision
  • Cardiology

In-Office and At-Home COVID Testing

COVID-19 RT-qPCR

Our saliva-based COVID-19 test detects active SARS-CoV-2 infection in patients with or without symptoms.

The test was approved by the FDA for Emergency Use Authorization (EUA) in June 2020.

  • The sensitivity of the test is 97.1% and the specificity is 98.2%.
  • We aim to provide results back within 48 hours of a completed test kit arriving at our lab.

Learn More
View our EUA

A Trusted Partner

Clinical and Industry Validation of our Solutions

Provider practices and healthcare systems trust us to deliver accurate and efficient genetic testing to their patients.

CAP-Accredited & CLIA-Certified

Our lab is state-of-the-art, CAP (College of American Pathologists)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified.

Licensed Across All 50 States

We completed the rigorous Clinical Laboratory Evaluation Program (CLEP) administered by the New York State Department of Health (NYSDOH) and have been issued its clinical laboratory permit in the category Genetic Testing – Molecular, making our services available across all 50 states in the U.S.