VSClinical

SeqOne is an AI-powered genomic analysis platform designed to help molecular laboratories, clinical teams, biologists, and geneticists transform complex next-generation sequencing data into fast, precise, and actionable clinical insights to support personalized medicine diagnostics. It streamlines end-to-end genomic workflows, from raw sequencing files to variant interpretation and reporting, by automating routine pipeline tasks, integrating seamlessly with lab systems, and using advanced AI models such as DiagAI to rank and highlight disease-relevant variants with explainable scores, reducing manual effort and turnaround time. SeqOne supports germline and somatic analyses across applications, including oncology, rare and inherited diseases, and infectious disease detection, combining premium annotation databases and standardized interpretation guidelines to ensure clinical-grade accuracy within an intuitive user interface that scales via secure cloud.

Geneyx Analysis is a comprehensive solution for next-generation sequencing (NGS) data that can scale the process of FASTQ to clinical reports for hospital and commercial labs. This advanced platform integrates machine learning and AI-based features to identify novel biomedical insights, while also improving diagnostic yields and turnaround times. By providing a fully transparent and intuitive solution, Geneyx Analysis enables clinicians and researchers to have complete control over data analysis and alleviates the complexities of regulating in-house bioinformatics pipelines. Protocols can be fully customized to accommodate gene panels, exomes, and genomes, and our comprehensive annotation engine supports the analysis of all genetic variants including structural and copy number variations as well as regulatory elements. Together, Geneyx Analysis automates the diagnostic process from sequencer to report, while creating a comprehensive resource for novel variant discovery.