For Molecular Diagnostics Companies

Modern Infrastructure for Your Entire Molecular Diagnostics Business

One platform for internal R&D pipeline decisions and external pharma data partnerships. Manifold unifies your clinical testing data so your teams and partners get secure, governed access to the insights they need.

3-4 months

to first data delivery

Days → Minutes

for model selection queries

50%+

reduction in manual data requests

Trusted by Leading Organizations

You're Not Alone

Untapped Revenue Potential

Valuable real-world genomic data from thousands of patients remains undermonetized due to lack of efficient pharma licensing infrastructure.

Slow Partnership Cycles

Each pharma partnership requires 6-12 months of legal negotiations and custom technical infrastructure, severely limiting deal velocity.

Disconnected Systems Hold You Back

Internal R&D teams and external partners need access to the same multimodal clinical testing data, but disconnected systems force you to manage everything separately—slowing down both.

"Manifold helps us prioritize speed and specialization. With their AI capabilities combined with our proprietary multi-modal data, FoundationInsights® powered by Manifold is resonating with customers and partners.”

Brian Clancy

Senior International Product Manager, Data Solutions & Partnerships, Foundation Medicine

Chosen by R&D Leaders

Broad Clinical Labs needed to deliver BGE and WGS sequencing data to customers on AWS, moving beyond simple file delivery. By partnering with Manifold, they now deliver data directly to AWS where customers browse QC data, variants, and files using AI. In addition, their customers can upload phenotypic data that automatically joins with genotype data—delivering far more value than traditional file delivery.

Foundation Medicine needed to accelerate drug development for biopharma partners using their comprehensive 800,000+ patient genomic dataset. FoundationInsights® 2.0, powered by Manifold, enabled this with natural language search and advanced analytics, giving partners a one-stop shop to rapidly identify patient cohorts, explore genomic alterations, and extract insights faster than ever before.

Indiana University SCCC needed to accelerate complex cohort queries across 28,000+ patient records and 81,000+ biospecimens that were taking weeks to complete. Manifold enabled them to cut query turnaround times from weeks to minutes, empowering researchers to independently generate feasibility assessments and complete multi-dimensional genomic queries while the BC^2 team handles increased request volume without adding headcount.

Champions Oncology needed a platform that could serve both their internal R&D teams and enable commercialization of their multi-omics dataset which includes PDX models with proteomics, WES, and RNA-seq data. They found a solution with Manifold that addresses both needs: a secure platform that scales from internal collaboration to external partner access, with Manifold's AI agents accelerating data evaluation and analysis across the board.

Indiana University SCCC needed to break down data silos across IUH, Regenstrief, and IU SCCC to integrate their EHR and other modalities into a unified research data commons. Manifold enabled the first-ever cross-institution collaboration through weekly EHR syncs, creating a place where researchers—even those with low technical expertise—can now ask natural language questions of over 3 million diagnoses, cut cohorts, and perform complex analyses that previously required weeks of manual data coordination.

University of Virginia Cancer Center needed to integrate their cancer registry data—including genomics, biospecimen, and clinical data—into a unified data commons, but data requests that used to take weeks or months were bottlenecking research. Manifold's AI-powered platform cut request turnaround times from months to minutes, enabling researchers to self-serve access to 60K+ patients and 10K+ biospecimens using natural language queries—unlocking far more research capacity.

Solutions

Fit-for-purpose solutions for clinical research leaders in cancer and rare disease.

Cancer Observational Study

Streamline legacy systems and manual processes with a single study and data management platform.

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Cancer Center Biobank

Reduce and turnaround time and increase productivity by connecting biospecimen data and clinical data in a single data management platform.

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Cancer Center Registry

Unify clinical and multimodal data on a modern platform to enable automated data preparation into a research-ready patient model.

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Rare Disease Registry

Answer research questions about diagnoses, treatments, and outcomes quickly and easily.

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One Platform for Internal R&D and External Data Partnerships

Accelerate Internal R&D

Bring multimodal data together so your teams can make faster pipeline decisions, design prospective studies, and identify biomarkers.

Unified access to genomic, clinical, and outcomes data

AI-assisted data exploration and analysis

Self-service access for bioinformatics teams

Molecular diagnostics companies using platform for both internal R&D and external commercial partnerships

Pharma-Ready Infrastructure

Secure, compliant, auditable data access that meets pharma ITand legal requirements out of the box

100% audit trail for all data access

Tiered access controls and permissions

Automated usage metering and billing

Pre-configured for pharma IT requirements

Leading CRO serving multiple pharma partners simultaneously through single infrastructure with tiered access controls

Scalable Data Operations

Serve internal R&D teams and external partners through a single platform — no incremental engineering required.

Onboard new partners in days, not months

Role-based access for internal teams and external collaborators.

Central management dashboard for all partnerships

Unified view across multimodal datasets.

One organization serves multiple pharma partners simultaneously, with self-service reducing manual data delivery requests by 50%+

Fast Time-to-Partnership

Go from first conversation to data delivery in 3-4 months, not 12-18 months

Pre-negotiated template agreements reduce legal cycles

Pharma-approved security & compliance out of the box

No custom engineering required for each partnership

One molecular diagnostics company reduced partnership setup time from days to minutes for model selection queries

Your Data, Multiple Use Cases

Internal R&D Pipeline Optimization

Unify multimodal data to accelerate pipeline decisions and biomarker prioritization

Prospective Study Design

Design and execute prospective studies with governed access to historical testing data

Pharma Licensing for Drug Development

License real-world genomic data for target discovery and biomarker identification

Companion Diagnostics Partnerships

Enable CDx development with real-world validation datasets

Real-World Evidence Generation

Support regulatory submissions with longitudinal patient outcomes

Clinical Trial Recruitment

Power patient identification and recruitment services

Is Manifold Right for You?

10K+ Patient Samples

Deploy in 3-4 months at a fraction of the cost. No multi-year engineering projects or maintenance fees required.

Data Partnership or R&D Modernization Goals

Active pharma partnership pipeline or strategic priority to modernize how teams access clinical testing data

Need for Scalable Infrastructure

Want to serve 3+ pharma partners without rebuilding infrastructure each time

Speed to Market Priority

Need to reduce partnership setup time from 12+ months to 3-4 months

Compliance Requirements

Need enterprise-grade security, audit trails, and governance for pharma partnerships

Get Started Today

Learn how Manifold can help you enable secure data sharing, accelerate partner evaluation cycles, and deliver governed analytics environments.

Setup complete in 3-4 months

Support multiple collaborators simultaneously

Enterprise-grade security & compliance

Flexible access models