GeoMx Spatial Transcriptomics
Best-in-class GeoMx SolutionFrom DCC files to pathway enrichment and beyond
Single Cell Gene Expression
From FASTQ to cell clusters and beyond
Gene Expression: RNA-seq
Complete guide to RNA-seq data analysis
NanoString: Gene & miRNA Expression
Visualize and collaborate on NanoString nCounter datasets
Gene Regulation & Anti-Sense: Small RNA-seq
Small RNA-seq data analysis designed for the biologist
Histone Mark & Transcription Factor: ChIP-seq
Comprehensive ChIP-seq data analysis
Chromatin Accessibility: ATAC-Seq
Genome-wide chromatin accessibility analysis
Sharing & Collaboration
Accelerate teamwork anywhere in the world
Knowledge Graph and Search
Data organized for semantic queries
COVID-19 Diagnostic Monitoring System
SARS-CoV-2 Viral Mutation Tracking
COVID Research Community
Global research analyzing COVID-19 genomic datasets
Immuno Oncology
Making discoveries on IO research
Breast Cancer
Identifying differentially expressed miRNAs in breast cancer
HIV
Transcriptional and genomic profiling study of HIV+ DLBCL
Diabetes
Discover and accelerate T1D
Multi-Omics Dataset
Explore multi-omics datasets in epigenetics research
Single Cell Data
Explore datasets with our Cell Ranger graph-based clustering
nanoString Gene Expression
Analyze your nCounter data in minutes
nanoString Mouse Glial Profiling Panel
Explore neuroinflammatory astrocyte subtypes in the mouse brain
RNA-Seq Data
Get started with bulk RNA-Seq data
Subscription and Pricing Comparison
Learn about Enterprise, Professional, and Academic subscriptions
Enterprise Offering
Expand the depth and reach of your scientific data teams
Begin exploring your analysis today! Now available to all NanoString users, sponsored for 1 year.
Register below to receive an nCounter Starter subscription, or upgrade to Professional.
If you are a scientist analyzing nCounter data, ROSALIND enables same day analysis results with a rich engaging user experience that saves valuable time and restores the thrill of discovery.
If you are a scientist analysing nCounter data, ROSALIND enables same day analysis results with a rich engaging user experience that saves valuable time and restores the thrill of discovery.
Scientists of every skill level can benefit from ROSALIND since no programming or bioinformatics skills are required. With powerful downstream analysis and collaboration, ROSALIND is a discovery platform and data hub connecting experiment design, quality control and pathway exploration.
ROSALIND automatically manages tens of thousands of compute cores and petabytes of storage to dynamically scale up and down for every experiment to deliver results.
Instantly share results with other scientists across the globe with audit tracking so everyone can focus on the interpretation not the processing.
Interconnect every stage of NGS data analysis to discover more than ever thought possible with collections of fragmented applications and tools.
Every scientist should have the freedom to perform advanced analyses without the dependence or delay of waiting on someone else to analyze their own data and miss what they know is there. Enjoy more than 50 knowledge bases all in one platform.
Find patterns across comparisons with advanced machine learning in Meta-Analysis.
Now you can easily process nCounter RCC files taken directly from the nCounter Digital Analyzer, or export a collection of experiments from nSolver to jumpstart your research and begin your visual discovery.
Evaluate gene signatures across nCounter experiments and public datasets. Gene signatures accelerate discovery by focusing on the genes, pathways and diseases of interest.
Discover, share and validate gene signatures using the Gene List Manager.
Automated contamination detection helps to identify data concerns before you invest hours into trying to diagnose results.
Sharing experiments and your insights with your project team and collaborators should not require offline, static screen captures or prints.
Every change is instantly available to each participant any where in the world with an audit trail reported on the activity feed.
Consistent, global collaboration on genomic data accelerates discovery and eliminates unnecessary complexity unifying your scientific expertise everywhere in the world.
ROSALIND Collaboration Spaces connects researchers within a virtual meeting room
Ever seen a genome browser look this good? There is simply no reason to settle for less.
Upgrade for access to all pipelines in Gene Expression, Gene Regulation, Chromatin Accessiblity and Protein Binding to visually experience interactive plots and interpretation, rather than eye-straining spreadsheets.
Tune the ROSALIND experience to match the way you discover.
Nicole Coufal, M.D., Ph.D
Assistant Professor and Pediatric Intensivist University of California San Diego and Rady Children’s Hospital
Long Do, Ph.D.
Senior Manager, Informatics
Samumed, LLC
Gary Hardiman, Ph.D.
Professor & Chairman in Food Systems Biology
Institute for Global Food Security
Health and Life Sciences School of Biological Sciences,
Queen’s University Belfast
Ted DeFrank
Chief Executive Officer & President
Active Motif
Amanda Laque
Staff Scientist
Scripps Research Institute
Michael Garabedian, Ph.D.
Professor, Department of Microbiology
Professor, Department of Urology
New York University Langone Health
Customize your ROSALIND experience by setting personal preferences for everyday use.
Scientists of every skill level benefit from ROSALIND since no programming or bioinformatics skills are required. With powerful downstream analysis and real-time collaboration, ROSALIND is the platform to empower your scientists and accelerate your discoveries.
Now available free of charge to all NanoString users for 1 year!