The startup operates a personal health and genomic data-sharing platform that connects users with researchers, enabling participation in studies on common and rare diseases. By allowing individuals to control their data and opt into research, the platform facilitates the collection of dynamic health and genetic datasets for personalized medicine.
Funding
$8.3M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
WVFounders
Product
Problem
The increasing volume, complexity, and variety of genomic data present significant challenges for researchers and clinicians. Existing technologies often struggle to efficiently store, retrieve, analyze, and interpret this data, hindering advancements in precision medicine and personalized healthcare.
Solution
Zetta Genomics offers XetaBase, a genomic data management and analysis platform designed to address the challenges of handling large-scale genomic datasets. Built on the open-source OpenCB platform, XetaBase provides a unified environment for storing, integrating, annotating, and analyzing genomic data alongside clinical and operational metadata. The platform's architecture enables efficient data management, rapid query response times, and scalable storage, facilitating the discovery of novel biomarkers and the development of targeted therapeutics. XetaBase supports a range of applications, from clinical diagnostics to population-scale genomic research, empowering users to unlock valuable insights and accelerate advancements in precision medicine.
Target Audience
The primary target audience includes clinical diagnostics laboratories, healthcare initiatives, biopharmaceutical companies, and research institutions involved in genomic research and precision medicine.
Features
- Genomic-native technology built on the open-source OpenCB platform
- Scalable storage and high-performance computing capabilities for handling large-scale genomic datasets
- Integrated clinical and variant data harmonization for optimized data accessibility and insights
- Advanced analytics and visualization tools for comprehensive data analysis
- Support for Nextflow workflows and Jupyter notebooks for customizable data processing and analysis pipelines
- Secure, cloud-based platform with role-based access control and data encryption
- Integration with public databases and third-party platforms via APIs
- Compliant with relevant regulatory standards, including MHRA and UKCA