When it comes to advanced data analysis, Rosalind offers a comprehensive solution that nSolver cannot match. Rosalind is continuously updated with no maintenance required, ensuring you always have access to the latest features. It also ensures gene pruning and normalization are done in the correct sequence, providing more reliable insights. With multiple pathways databases and p-value support, Rosalind delivers deeper analysis, while its real-time collaboration tools and shared libraries make teamwork seamless. Additionally, Rosalind offers robust QC and meta-analysis tools to ensure high-quality results every time.
Scientists of every skill level can benefit from ROSALIND since no programming or bioinformatics skills are required. With NanoString nCounter, scientists have full control from the lab to powerful downstream analysis, collaboration, and pathway exploration.
As NanoString's strategic partner for data analysis, ROSALIND brings a seamless and enhanced nCounter experience to your laboratory. Our platform integrates directly with NanoString technologies to deliver a streamlined workflow and superior data analysis capabilities, specifically tailored for nCounter data, including RAW RCC files as well as processed data exports.
This unique experience features custom normalization, advanced cell type profiling, and effective pruning of low expressors—all designed to refine data clarity and improve analytical accuracy. With intuitive interfaces and real-time processing, Rosalind makes complex data analyses accessible and actionable for all levels of scientific research.
Custom pruning of low expressors is vital for researchers as it significantly reduces background noise and enhances the clarity of the data. By focusing on genes with higher expression levels, scientists can avoid misleading results caused by random fluctuations in low-expressed genes.
ROSALIND automates this process, integrating advanced algorithms that intelligently identify and eliminate these low expressors, streamlining workflows and improving data quality.
Leverage the power of expert-level bioinformatics with the sophistication of ROSALIND's Custom Normalization. Our platform brings GENORM's advanced capabilities directly to your fingertips, allowing you to effortlessly identify and select the most stable reference genes for precise normalization.
By guiding you to the optimal genes and enabling the export of your selections for consistent application across multiple analyses, ROSALIND empowers your research with the methodologies championed by leading bioinformatics teams, ensuring your data's integrity and reproducibility.
Ensure analytical consistency across your team with ROSALIND's export feature, designed to align your normalization process efficiently. This capability empowers researchers to share selected normalization probes, providing a foundation for uniform analysis within collaborative projects.
Perfect for teams who value the precision of synchronized normalization or require the flexibility to conduct advanced offline bioinformatics analysis. With this feature, you can easily export data, maintain consistent normalization standards, and uphold the integrity of your research, regardless of the complexity of your analytical workflows.
Rosalind Intelligence goes beyond the basics to amplify the impact of your targeted gene panel. It not only increases the investment value but also enriches your research with deep, often missed connections. Shift from a narrow view to a panoramic perspective of biological interactions, as nSolver’s limitations are surpassed by Rosalind's expansive interpretation.
Harnessing the power of generative AI that’s grounded in biological truth with the Rosalind Knowledge Graph for rich and insightful Literature Reviews, produced in seconds on your target genes of interest. Explore correlations to all available nCounter data from the public repositories. Discover hidden links within your data that drive groundbreaking findings and elevate your research's impact.
With a team of specialists whose expertise eclipses the basic support offered elsewhere, Rosalind provides an unmatched level of nCounter knowledge. Our dedicated experts, well-versed in the nuances of nCounter technology, remain ahead of the curve, focusing on your needs while NanoString continues to innovate the platforms of tomorrow. Partner with us for industry-leading insights and support that's as advanced as your research.
Coupled with the domain expertise of our PhD-level Customer Success team, Rosalind delivers a symbiosis of technical acuity and deep scientific understanding. This dual approach ensures that your nCounter analysis is not only technically sound but also strategically aligned with the nuances of your research domain.
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Explore the innovative studies and publications by our nCounter users. It's inspiring to witness the impactful research conducted on ROSALIND, leading to new scientific discoveries and advancements. Join the ranks of our esteemed community of scientists making waves in the field of genomics.
Soon, Rosalind Intelligence will show correlations and anti-correlations of your datasets to libraries of public nCounter datasets, validating your hypotheses and results as you plan the next stage of your research.
Unlock the full narrative of your nCounter data by integrating with diverse multiomics layers of data. Rosalind’s meta-analysis empowers you to compare nCounter datasets with precision or to weave them into a broader multi-omics tapestry with Rosalind Intelligence to discover and interpret patterns in multi-omics expression and regulation.
This integrative approach ensures that your nCounter insights are not isolated but are considered in the context of the complex biological systems they inhabit, offering a holistic understanding that drives innovative research and serves a data mining foundation for future insight harvesting.
ROSALIND Collaboration Spaces connects researchers within a virtual meeting room
Gene Expression, Gene Regulation, Chromatin Accessiblity and Protein Binding are best experienced visually with interactive plots and interpretation, rather than eye-straining spreadsheets.
STARTING AT $99 PER MONTH (Select your Instrument Type)
Available for Academic Research Institutions, Academic Medical Centers and non-Profit Research Institutions
STARTING AT $149 PER MONTH
Available for Academic Research Institutions, Academic Medical Centers and non-Profit Research Institutions
Need RNA-seq (bulk and Single-Cell), ChiP-seq, ATAC-seq, or miRNA-seq, too? Learn about our special Academic Pricing for Multi-Omics
Looking for solutions to help consistently manage research for your entire lab at significantly reduced costs? Learn about our Academic Team Pricing.
For commercial sales, learn more here, or contact us for quotes and custom configurations.
