Speeding the Diagnosis of Rare Genetic Disorders with
Millions of children around the world are born each year with severe genetic disorders. Many
Founded under Baylor College of Medicine, in collaboration with Baylor Genetics, the Undiagnosed Disease Network, and the Chan Zuckerberg Initiative, MARRVEL AI integrates the power of our MARRVEL database with our advanced AI algorithm, creating a unified solution for precise genetic analysis.
State-of-the-art algorithm analyzes data with unparalleled accuracy, reducing errors and increasing confidence in your results.
Experience rapid analysis, enabling quicker decision-making and accelerating your research and clinical workflows.
A few samples vs. massive datasets, MARRVEL AI scales effortlessly to meet your needs without compromising performance.
Achieve significant savings while increasing quality—reducing costs while maximizing value for your research and clinical needs.
Designed with you in mind, our intuitive platform ensures a seamless experience for professionals across various fields.
We prioritize data security and compliance, adhering to the highest industry standards to protect your sensitive information.
After our publication in the New England Journal of Medicine AI, MARRVEL AI has seen positive reception and coverage in numerous articles.
Millions of children around the world are born each year with severe genetic disorders. Many
Diagnosing rare Mendelian disorders is a labor-intensive task, even for experienced geneticists. Investigators at Baylor
Using an artificial intelligence (AI) model that was trained on millions of variants from identified
AI-MARRVEL (AIM), a new artificial intelligence (AI) system, was trained using samples diagnosed by experts
Whether you have questions about our platform, want to discuss partnership opportunities, or simply need more information, our team is ready to help. Reach out today, and let’s explore how MARRVEL AI can empower your mission in precision genomics.