The company provides 30×‑genome sequencing via an at‑home saliva kit, delivering raw dataFASTQ/BAM/VCF) and AI‑generated health reports covering disease risk, pharmacogenomics, carrier status, and ancestry. Reports are automatically re‑analyzed as new evidence emerges and are accessible through a HIPAA‑compliant, FHIR‑compatible cloud portal that integrates with EHR and research systems.
Funding
Funding not disclosed
Founders
Product
Problem
Many consumers and healthcare providers lack affordable access to high‑coverage whole genome sequencing that delivers clinically actionable insights, limiting early detection of genetic risk factors and personalized health planning.
Solution
The company offers a 30× whole genome sequencing service that generates complete raw genomic datasets (FASTQ/BAM/VCF) and delivers AI‑enhanced health reports. Their proprietary analytics pipeline interprets variants for disease risk, pharmacogenomics, carrier status, and ancestry, presenting findings in a clinician‑ready dashboard. Reports are updated automatically as new scientific evidence emerges, ensuring users receive the latest actionable recommendations without re‑ordering tests. Data are stored in a secure, HIPAA‑compliant cloud environment with role‑based access controls and API endpoints for integration with electronic health records or research platforms. The end‑to‑end workflow—from at‑home saliva kit collection to data delivery—streamlines the genomic testing experience for both individuals and professionals.
Target Audience
Primary customers are health‑conscious individuals seeking preventive genomic insights and clinicians or research institutions that require high‑resolution genomic data and automated interpretation for patient care or scientific studies.
Features
- 30× coverage whole genome sequencing using Illumina NovaSeq technology for high accuracy and uniformity
- Delivery of raw sequencing files (FASTQ, BAM, VCF) plus processed variant calls for downstream analysis
- AI‑driven interpretation engine that prioritizes clinically relevant variants across > 7,000 genes
- Structured health reports covering disease susceptibility, drug response, carrier status, and ancestry insights
- Continuous reanalysis pipeline that incorporates the latest genomic research and updates reports automatically
- Secure, encrypted cloud portal with FHIR‑compatible API for seamless EHR or LIMS integration
- End‑to‑end sample logistics: at‑home saliva collection kit, temperature‑controlled shipping, and real‑time tracking
- Compliance with GDPR, HIPAA, and ISO 27001 standards for data privacy and security