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MyOme

Clinical-grade genome sequencing for disease risk

Overview

MyOme provides clinical-grade whole genome sequencing to assess disease risk for individuals and families. It uses comprehensive genome data combined with AI and machine learning to generate integrated disease risk scores that update over time as lifestyle changes occur, delivering actionable insights for lifelong health management. The company differentiates itself by offering a single, detailed genetic test that yields evolving, lifetime risk evaluations rather than a one-off report, targeting both common and rare diseases. Its goal is to enable earlier health interventions and better disease management through personalized, data-driven genetic information.

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About MyOme

Simplify's Rating
Why MyOme is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

Data & AnalyticsAI & Machine LearningBiotechnologyHealthcare

Company Size

51-200

Company Stage

Series B

Total Funding

$23M

Headquarters

Palo Alto, CA

Founded

2017

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Simplify's take

What believers are saying

  • November 4, 2026 SickKids validation deepens rare-disease utility and strengthens clinical credibility.
  • October 8, 2026 CASRcade funding from BridgeBio opens a repeatable sponsored-testing growth lane.
  • September 24, 2026 Oracle global availability broadens access and supports international enterprise sales.

What critics are saying

  • Natera controls Zenith commercialization, making MyOme dependent on one dominant channel partner.
  • MyOme's model hinges on complex payor reimbursement and clinician adoption by 2027.
  • If Natera or Oracle shifts terms, MyOme loses distribution and infrastructure leverage quickly.

What makes MyOme unique

  • MyOme combines whole-genome sequencing, methylation, and polygenic scoring in one clinical report.
  • Its November 4, 2026 SickKids license expands rare-disease interpretation with proprietary methylation signatures.
  • Oracle worldwide deployment gives MyOme global compute for reanalysis as genomic science advances.

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Funding

Total Funding

$23M

Below

Industry Average

Funded Over

1 Rounds

Notable Investors:
Series B funding is typically for startups that have proven their business model and need more funding to expand rapidly—often by entering new markets or adding more products. Investors are usually venture capital firms that specialize in later-stage investments.
Series B Funding Comparison
Below Average

Industry standards

$35M
$30M
$45M
$65M
$100M

Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Unlimited Paid Time Off
  • Remote Work Options
  • Hybrid Work Options
  • Professional Development Budget
  • Company Social Events

Company News

PR Newswire
Oct 8th, 2026
MyOme launches free genetic testing programme for families affected by ADH1

MyOme has launched CASRcade, a no-charge cascade genetic testing programme for US families affected by Autosomal Dominant Hypocalcemia Type 1 (ADH1). The programme, sponsored by BridgeBio, offers free genetic testing and counselling to biological relatives up to fourth degree of individuals with confirmed ADH1. ADH1 is a rare genetic form of hypoparathyroidism caused by variants in the CASR gene. Because it follows an autosomal dominant inheritance pattern, each child of an affected parent has a 50% chance of inheriting the condition. Healthcare providers can enrol patients through MyOme, who will then identify eligible relatives for testing. MyOme will perform targeted genetic sequencing to determine whether relatives carry the same CASR variant, facilitating earlier diagnosis and proactive care.

PR Newswire
Sep 24th, 2026
MyOme partners with Oracle to deliver genomic risk prediction worldwide

MyOme, a clinical whole-genome analysis company, announced its predictive genomic insights platform is now available worldwide, running on Oracle Cloud Infrastructure. The California-based firm has joined Oracle PartnerNetwork to expand access through the Oracle ecosystem. MyOme sequences individuals' whole genomes and uses OCI's computing to analyse millions of genetic variants alongside clinical risk factors. The platform evaluates risk for rare and common diseases, producing AI-driven polygenic risk scores for conditions including coronary artery disease, type 2 diabetes, prostate cancer, and breast cancer. Unlike traditional genetic testing that reads narrow gene panels, MyOme's whole-genome approach allows one sample to produce broad clinical insights that can be re-queried as patients' health evolves and science advances.

PR Newswire
Apr 21st, 2026
MyOme appoints Sam Roosz and Dr Ravi Thadhani to board of directors

MyOme, a genomics innovation and risk modelling company, has appointed Sam Roosz and Dr Ravi Thadhani to its board of directors. The appointments strengthen the company's expertise in healthcare technology, data portability and regulatory strategy as it expands its AI-powered whole-genome healthcare platform. Roosz is co-founder and CEO of Crescendo Health and previously co-founded Datavant, building the nation's largest health data ecosystem. Dr Thadhani serves as executive vice president of clinical affairs and chief medical officer at Cedars-Sinai, bringing over 30 years of experience in academic medicine and regulatory strategy, including FDA advisory board service. MyOme's platform uses advanced AI and integrated risk modelling to deliver genomic insights across clinical care and research applications, covering cardiometabolic, oncology, rare conditions and pharmacogenomics.

The Astorian
Apr 21st, 2026
MyOme strengthens board with appointment of two healthcare leaders.

MyOme strengthens board with appointment of two healthcare leaders. PR Newswire Today at 8:24am PDT MENLO PARK, Calif., April 21, 2026 /PRNewswire/ - MyOme, a leading genomics innovation and risk modeling company, today announced the appointment of Sam Roosz and Dr. Ravi Thadhani to its Board of Directors. The two executives bring deep expertise spanning healthcare technology, data portability, clinical trials, population health, and regulatory strategy - strengthening MyOme's position as it expands its AI-powered whole-genome healthcare platform. Sam Roosz is Co-Founder and CEO of Crescendo Health, where he is building a patient-centered platform that enables individuals to securely contribute their complete health history to medical research, and was previously Co-Founder of Datavant, where he helped build the nation's largest health data ecosystem - enabling secure data linkage across providers, researchers, and public agencies. His track record in enterprise partnerships and high-growth execution will guide MyOme as it scales whole-genome solutions across health systems, life sciences, employers, and population health networks. "MyOme is unlocking the clinical value of the whole genome and multianalyte analysis in a way that is actionable for patients and providers. Delivering integrated, validated genomic insights at population scale has the potential to fundamentally reshape how healthcare is delivered. I'm excited to support the company's next phase of growth." - Sam Roosz Dr. Ravi Thadhani, Executive Vice President of Clinical Affairs and Chief Medical Officer at Cedars-Sinai, is a nationally recognized leader with more than 30 years of experience spanning academic medicine, clinical operations, and regulatory strategy. He has held senior leadership roles at Emory University, Harvard Medical School and Mass General Brigham, and brings extensive firsthand experience on data safety monitoring and guiding diagnostics through FDA approval pathways - directly aligned with MyOme's evidence-building and commercialization strategy. "Whole-genome-powered insights represent one of the most meaningful opportunities to transform how disease is understood, diagnosed, and managed. MyOme's integrated approach - combining monogenic and polygenic insights with strong clinical evidence and regulatory rigor - positions the company to drive significant impact across the healthcare system."- Dr. Thadhani Matt Rabinowitz, PhD, Co-Founder and Executive Chairman of MyOme, emphasized the importance of the newly appointed board members. "Sam has scaled influential health-data platforms, and Ravi has led major clinical organizations while guiding innovative diagnostics through FDA pathways. Their combined expertise will be invaluable as whole-genome and multiomic intelligence becomes foundational to modern medicine." MyOme's whole-genome platform uses advanced AI and integrated risk modeling to deliver actionable genomic insights across clinical care and research applications - spanning cardiometabolic, liver, kidney, cognitive disease, oncology, rare conditions, pharmacogenomics and beyond. Sam Roosz is co-founder and CEO of Crescendo Health, a healthcare technology company that provides the life sciences industry with comprehensive insights into the real-world health outcomes of consenting research participants. Sam previously co-founded and served as GM of Life Sciences at Datavant, the leading provider of de-identification and linking solutions for health data. Sam received a degree in Molecular and Cellular Biology from Harvard and holds an MBA from the Stanford Graduate School of Business. Dr. Thadani Ravi Thadhani, MD, MPH, has more than 30 years of experience as a general and specialized internal medicine physician, a clinical and translational investigator, and a leader in life sciences, healthcare, and academia. He is the author or co-author of more than 300 published scientific manuscripts and has received several awards including the John P. Peters Award from the American Society of Nephrology. He has extensive regulatory experience having served on the FDA's Cardiovascular and Renal Drugs Advisory Board for many years. In 2025 he was elected into the National Academy of Medicine. He is the former executive vice president for health affairs of Emory University, overseeing a large hospital system and schools of medicine, nursing, and public health. Previously, Dr. Thadhani was a professor at Harvard Medical School and Chief Academic Officer and Dean for Faculty Affairs at Mass General Brigham... He was formerly the chief of nephrology at Massachusetts General Hospital, served on the board of the Broad Institute of MIT and Harvard University and was Chair of the National Kidney Foundation Clinical Research Committee. He also served as chair of multiple NIH trial Data Safety Monitoring Boards and was a member of the FDA Cardiovascular and Renal Drugs Advisory Committee. Dr. Thadhani earned his Doctor of Medicine degree from the University of Pennsylvania School of Medicine, his Master of Public Health degree from the Havard T.H. Chan School of Public Health, and his bachelor's degree from the University of Notre Dame. He also received a certificate of business leadership at the Graduate School of Business at Stanford. About MyOme MyOme is a clinical whole genome analysis company helping families understand their risk for diseases. As a leader in polygenic and AI-based integrative risk modeling, MyOme leverages the power of the whole genome and clinical data for a lifetime of meaningful and actionable insights. These capabilities can dramatically reduce healthcare costs and improve outcomes by catching disease earlier and taking steps to delay or stop their onset. Certified under the Clinical Laboratory Improvement Amendments (CLIA) and certified by the College of American Pathologists (CAP), MyOme is based in Menlo Park, California. SOURCE MyOme, Inc This is a paid placement. For further inquiries, please contact PR Newswire directly.

PR Newswire
Mar 12th, 2026
MyOme launches Zenith with Natera, adds long-read methylation analysis for rare disease diagnostics

MyOme, a clinical whole-genome analysis company, has announced its integration of methylation signatures into its whole-genome platform at the American College of Medical Genetics and Genomics Annual Meeting. The technology aims to reduce the average five-year diagnostic delay for rare disease patients. MyOme is partnering with Natera to launch Zenith, a premium exome and genome testing solution now available for commercial orders across the United States. The platform combines DNA sequencing with methylation pattern analysis using long-read sequencing, enabling clinicians to resolve variants of uncertain significance and imprinting conditions. Starting in Q2 2026, methylation analysis will be automatically integrated into all eligible rare disease exome and genome analysis orders. MyOme will initially perform targeted confirmation for select conditions before expanding to additional disease areas.

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