Informatics to help guide decisions
Managing, and ultimately interpreting, the significant quantities of variant data produced by next-generation sequencing (NGS) and cytogenetics workflows presents a formidable challenge. In oncology specifically, the wide range of variants in tumor and blood samples presents challenges for efficient, accurate, and thorough analysis of cancer-relevant data.
Oncomine informatics helps you:
- Prioritize variants, find the relevant few
- Calls variants, identify and annotate cancer drivers
- Quickly create custom, lab-generated reports; integrate NGS and cytogenetics data for myeloid cancer reporting; and support oncologists in making informed treatment decisions
Dependable informatics for discovery and decisions
The Oncomine Informatics workflow ensures high quality data, prioritizes and annotates driver variants, and completes with software for clinical decision support to link relevant biomarkers to labels, guidelines, and clinical trials..
Streamlines sequencing runs and creates BAM files
Annotate and filter
Calls variants, identifies and annotates cancer drivers
Decision support tool
Links variants to relevant evidence
Intuitive, web-based interface through the Torrent Browser makes it fast and easy to plan, monitor, and view sequencing run results to enable high quality data for analysis.
Simplify your bioinformatics path to discovery with Ion Reporter Software. By helping to remove barriers in NGS data analysis, this software enables you to focus on finding the biological meaning of your data.
Oncomine Reporter produces clear and concise reports by linking relevant biomarkers with information from targeted therapies, guidelines, and global clinical trials.
Enabling a powerful set of analysis functions that compute gene expression signatures, clusters, and gene-set modules, Oncomine Platform Software automatically extracts biological insights from data.