Genoox provides researchers with a comprehensive end-to-end solution, making it faster and easier for researchers to uncover hidden signals and complex relationships between diseases and prioritized genes by applying advanced proprietary tools.
We collect data from millions of in-house and public records applying multiple variant callers and a robust annotation engine. Utilizing Genoox, researchers can easily apply best-practice guidelines through clinical decision support tools, track outcomes for quality improvement and share data and analyses with collaborators inside the organization or with external partners.
Our platform is cloud based and scalable to growing needs. we seamlessly integrate to existing systems and databases, allowing researchers to manage, analyze, and deliver results without the need for complicated and costly infrastructure investments.
Compare samples and cross information
Maximizing variant detection
Data that works for you
Achieve greater insights using existing processes
Increase predictions and scoring
Insightful interpretation - Delivered.
Fast, Efficient, Dynamic
The range of data types supported, the ease of querying and the robust scalability of the underlying cloud-based technologies allow us to handle ever-growing genome sequence database challenges providing meaningful insights in seconds. The Genoox robust query engine supports researchers to make the most out of their data and perform genome wide association studies to receive rapid genomic insights.
We maximize the number of high-value variants for your research project by combining multiple variant callers, advanced analytical tools and integrated content, analyzing each variant for its impact on protein function, conservation and frequency in a population.
Variants are annotated utilizing hundreds of data sources, from simple annotation to clinical evidence data utilizing a variety of data sources e.g. ClinVar, GWAS Catalog, dbSNP, OMIM and more.
To store and analyze genetic data efficiently, we provide a coherent picture using a complete and customizable bioinformatics pipeline from the sequence level to a report based on an optimized data management solution. Our pipeline is constantly validated against thousands of public datasets in addition to private data sets.
We apply unique machine learning algorithms delivering prediction tools and confidence scoring based on the type of variant and multiple assessment metrics.
Genoox provides automated sharing and reporting tools covering Genes, Exons, Transcripts and targeted regions, leveraging an extensive curated knowledge base, comprehensive analysis, insightful interpretation, and precise reporting. Reports generated can be branded, customized, viewed, printed, and shared with management, fellow researchers or technical leads.
We provide researchers with an end to end data-driven ecosystem. Our cloud based platform and dynamic modeling provides organizations full flexibility to address changing needs and requirements and eliminate the need for costly infrastructure investments.