Mavatar Discovery
From Complex Data to Precision Insights - in Hours, Not Months
With our research platform, Mavatar Discovery, you never start from scratch. Log in to a “set table” of ready-to-use biological networks and context - accelerating disease research and drug discovery from day one.
Introduction
What if researchers could uncover new drug targets, biomarkers, and disease mechanisms in hours, not months?
Now they can!
Mavatar Discovery is now available, delivering high-confidence, biologically grounded insights from large-scale transcriptomic data - with speed, clarity, and scientific rigor.
A new starting point for research.
Mavatar Discovery is a next-generation SaaS platform designed for researchers, pharmaceutical companies, and academia to accelerate disease and drug research.
It enables deeper, faster, and smarter insights through advanced, data-driven exploration of publicly available transcriptomic data.
Key benefits
Explore ways to shape meaningful choices that can transform your future.
Speed
From Months to Minutes
Analyze thousands of transcriptomic datasets and uncover meaningful biological patterns in minutes.
Simplicity
No Code Required
Skip the technical setup. Visualize complex gene networks instantly, without writing a single line of code.
Intelligence
Context-Rich Insights
Explore context-specific gene networks, functional enrichment, and overlapping disease pathways — all with traceability back to the source data.
Clarity
Actionable, Ready-to-Use Outputs
Get enriched, reproducible results you can directly apply to target discovery, biomarker validation, and translational research.
How it works
From Questions to Answers - in Four Simple Steps
With Mavatar Discovery, you don’t start from scratch. Our platform brings you straight to biologically meaningful networks and ready-to-use insights. Here’s how it works:
01
Select Your Focus Area
Choose from a growing library of tissues, diseases, and conditions curated for high research impact.
02
Explore Interactive Networks
Visualize gene correlations, pathways, and cross-disease overlaps with intuitive, interactive tools.
03
Compare and Contextualize
See how genes of interest behave across different tissues, conditions, or diseases.
04
Apply Your Findings
Download results, integrate with your workflows, and take discoveries forward.
Who it's for
Unlock great opportunities and turn potential into success.
Pharma & Biotech R&D Teams
De-risk discovery pipelines and accelerate therapeutic target identification.
Academic & Clinical Researchers
Move from raw data to publication-ready insights, faster than ever.
Translational Medicine Groups
Validate biomarkers and stratify patients with precision.
Contract Research Organizations (CROs)
Deliver high-value results to clients without building new infrastructure.
Licenses & Access Options
Flexible licensing tiers to fit your research needs
From first exploration to full integration in your workflows.
Free trial
For those trying out our features
Free 30-day trial
- Instant access for any user who creates an account
- Limited access - includes two selected, limited network - based on two mice tissue models; lung and liver
- Explore platform features and workflow before upgrading to a full license
- Onboarding pdf and video available
- Standard support
Academic/ Research
Contact us
- Upon registering with a valid academic email address - Full access to all networks with curated datasets, context-specific gene networks, cross-disease comparison, and functional enrichment tools
- Designed for academic researchers and smaller research groups
- Includes standard support and optional 1:1 digital platform onboarding
Professional
Contact us
- Full access to all networks with curated datasets, context-specific gene networks, cross-disease comparison, and functional enrichment tools
- Tailored for pharmaceutical R&D, CROs, and translational medicine teams
- Includes a 1-hour expert session/year with a Mavatar scientist to support your research goals, demonstrate advanced workflows, and provide tailored platform guidance
- Option to add up to 10 seats/users
- Priority support, dedicated 1:1 onboarding
Enterprise
Contact us
- Full access to all networks with curated datasets, context-specific gene networks, cross-disease comparison, and functional enrichment tools
- Ideal for large-scale organizations with specific workflow needs
- Option to add unlimited number of seats/users
- Includes a 2-hour expert session per year with a Mavatar scientist to support your research goals, demonstrate advanced workflows, and provide tailored platform guidance
- Dedicated account management and strategic consultation
- Priority support, dedicated 1:1 onboarding
Frequently Asked Questions
Mavatar Discovery
Mavatar Discovery is a next-generation SaaS platform designed for researchers, pharmaceutical companies, and academia to accelerate disease and drug research. It enables deeper, faster, and smarter insights through advanced, data-driven exploration of publicly available transcriptomic data.
Mavatar Discovery is designed to support:
- Pharmaceutical & Biotech Companies looking to optimize drug discovery and clinical trials.
- Contract Research Organizations (CROs) seeking data-driven insights for trial efficiency.
- Academic & Translational Researchers investigating disease mechanisms and biomarker discovery.
Mavatar Discovery’s core design does something unique: it integrates vast amounts of published transcriptomic data into a single, cohesive data resource. Large-scale integrated analyses are performed by Mavatar a priori. When a researcher logs in, they arrive at a set of ready-to-use tools and resources.
Analytical platforms elsewhere typically offer a set of tools allowing differential expression, clustering, heatmaps and others. While these tools are useful, Mavatar Discovery leapfrogs the user past these initial analyses, where biologically meaningful networks and context are already in place to explore.
For example, a researcher working with our breast or lung cancer resources doesn’t just access single datasets, but integrated networks based on training across hundreds of datasets and tens of thousands of patients. The platform also enables cross-references: studying lung cancer, you can simultaneously compare cancer related findings with with fibrosis, long COVID, or asthma to reveal overlapping mechanisms and pathways.
With Mavatar Discovery, researchers can both dive deep into disease-specific networks and explore tissue-wide patterns. The result is a platform that makes it faster, easier, and more powerful to identify new biomarkers, understand disease mechanisms, and uncover potential therapeutic targets.
Mavatar is powered by rich, fast-growing data sources from the global scientific community, such as Gene Expression Omnibus, The Cancer Genome Atlas, CellxGene, Single Cell Portal and others.
At the core of Mavatar Discovery is built on DINA (Deep Integrated Network Analysis), our proprietary framework built on 20+ years of scientific expertise. DINA integrates and analyzes thousands of transcriptomic datasets to model disease mechanisms at a systems level-delivering:
- Gene level networks by tissue and disease
- Functional enrichment tools with full traceability back to original datasets
- Overlapping networks across diseases for broader insights
- You get curated, structured results—not just raw data or pre-packaged database queries.
- New features and capabilities added continuously as we shape the future of research
Our approach also ensures high reproducibility, enables more accurate translation between animal and human studies, allows us to compare different diseases affecting the same tissue, and how the same disease presents in different tissues etc.
Mavatar Discovery helps you:
- Identify novel biomarkers and therapeutic targets
- Understand disease biology across tissues and conditions
- Explore complex gene interactions with ease
It’s a complete, cloud-based solution that transforms months of research into hours of actionable insights-ready to use from day one.
- Free Trial: Anyone can sign up for a 7-day Free Trial License with limited access.
- Full License: Annual license agreements range from $18,000 to $25,000 per year, depending on user type.
- Additional Users: Extra seats can be added for an additional fee.
- Contract Terms: Standard contract period is 1 year with automatic renewal.
Mavatar Discovery includes:
Single-Cell UMAP
Projects every cell in a single-cell RNA-seq experiment onto a 2-D map where closeness reflects transcriptomic similarity. By removing the need to juggle stand-alone UMAP apps, this feature speeds hypothesis generation and keeps biological context visible.
Use case: In a tumor atlas, a researcher selects a cell interaction network and instantly sees its clusters.
Thorough Gene & GSE Descriptions
Every node and dataset card now carries a plain-language summary and the experimental design behind the GEO Series (GSE). Context that once lived in scattered tabs is embedded beside the graph, cutting literature-lookup time and reducing annotation errors.
Use case: While exploring synaptic-plasticity networks, a neuroscientist immediately learns that GSE12345 used sleep-deprived mice, prompting her to control for circadian effects.
Dual-Network Union Analysis
Loads any two gene-interaction networks, and the viewer highlights shared hubs, unique edges, and enriched pathways in real time. This one-click comparison replaces manual scripts and spreadsheets, letting you instantly spot, for example, condition-specific rewiring.
Network Similarity Scatter Plot
This panoramic view lets you discover related datasets, detect outliers, or build meta-analysis cohorts without laborious pairwise tests.
DINA Functional Enrichment Chart
Quickly understand the significance of your findings and continue exploring your research question with our DINA Functional Enrichment Chart.
DINA Network Sub-Graph
Visualize subnetworks in seconds in the Mavatar Discovery canvas. All based on our proprietary DINA Network model.
And much more to come...
That’s just for now - Mavatar Discovery is just getting started, so expect continuous improvements and new features to be released going forward. Or better yet - be a part of the development and join us as an early user and make your voice heard!
Mavatar Discovery is a cloud-based platform accessible through a secure web interface. Users can log in, explore networks, and run analyses directly from their browser.
User can export their findings to png and svg (vector graphics). They can also customizable coloring and layout including pre-set themes that can match publication graphic requirements etc.
Yes, users can securely upload gene sets from e.g. their differential expression analysis to explore in the platform.
Depending on the complexity of the query, results can be generated in seconds to hours, significantly reducing the time required for traditional analysis. Is the tissue / disease you are interested in not precalculated in Mimer Discovery yet? Contact us and we will be happy to arrange a project together for a custom data survey and network construction.