nCounter® Data Analysis Solutions

Is an integrated analysis platform for storage  and custom QC/normalization, of nCounter data. It generates highly tailored exports, basic statistical outputs, and publication-quality figures quickly and easily with no incremental cost or need for bioinformatics expertise.

• Recommended QC on each sample
• Tunable normalization and fold-change measurements
• Statistical significance testing
• Comprehensive and detailed searches from anywhere in the application
• Compatible with standard analysis programs including Ingenuity Pathway Analysis, Partek Genomics Suite, BioDiscovery Nexus Copy Number, Advaita iPathwayGuide

ROSALIND is cloud-based, runs in a web browser, and provides an intuitive experience that’s designed with life scientists in mind. There is no software to install, and it’s always up-to-date. You don’t have to be an expert in statistics or bioinformatics. You can process nCounter RCC files directly in ROSALIND or start from a collection of experiments exported from nSolver. There are guided modules for normalization, QC, pathway analysis, differential expression, gene set analysis and PlexSet/multi-RLF support

Learn more here: ROSALIND

ROSALIND helps you get the most out of your nCounter data with:

• An intuitive user interface
• Interactive charts and figures
• Integration with 50+ knowledge bases enabling deep exploration of data sets
• Data-sharing with collaborators inside and outside your organization
• nCounter customers can access ROSALIND free of charge at https://www.onramp.bio/nanostring.

For questions regarding using ROSALIND, please contact support@rosalind.bio.