Power Drug Discovery and Development with DNAnexus
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MOVE FASTER, DIG DEEPER
- Ingest, unify, and manage your data quickly with out-of-the-box integrations and pre-built workflows. Conduct powerful analyses with an AI/ML-ready environment that provides a comprehensive command line experience to technical users.
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POWER R&D
- Enable your internal and external data stakeholders with large-scale dataset offerings, scalable data management capabilities, comprehensive collaboration tools, and an intuitive UX that serves users of all technical backgrounds.
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REDUCE RISK
Support your IT teams with secure, GxP-compliant solutions that are seamlessly implemented by our team of in-house experts. We’ll ensure that you never fall out of compliance and that you can tackle any challenge.
Partnering with the world's leading biomedical organizations
- Unify Multimodal Data
- Analyze at Scale
- Boost Clinical Trial Data Value
- Supercharge Collaboration
- Generate Insights
Unify Multimodal Data
Unify Multimodal Data
Intuitive clinico-omics data management
Quickly integrate and manage your multimodal data and metadata, including omics, phenotype, clinical, and imaging data.
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Automatable Data Unification
Integrate your precision health data and associated metadata in a FAIR and compliant way. Improve efficiency through data ingestion automation. -
Data Organization with a Full Audit Trail
Streamline and safeguard your operations with project-level data management tools, full audit-trails, and data lineage tracking. -
Extensive Instrument and Software Integration
Stream data from sequencing instruments, push and pull data from ELN and LIMS software, and send data to popular data analysis and visualization programs.
Analyze at Scale
Analyze at Scale
Robust, production-scale analysis
Process your data with ease with our pre-built pipelines or using your own custom tools. Automate your workflows to process data at scale.
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Streamlined Analysis Workflows
Create custom, automatable analysis pipelines in WDL, Nextflow, or Docker workflow languages to standardize and deploy new methods. -
Out-of-the-Box Tool Library
Quickly implement analysis pipelines using prebuilt tools for a variety of applications, including whole genome sequencing, bulk RNA-seq and proteomics, single cell analysis, and more. -
Customizable Functionality that is ML-Ready
Customize analyses with a robust suite of command tools, including R and SQL interfaces, built-in Jupyter environments, and ML frameworks, such as TensorFlow and PyTorch.
Boost Clinical Trial Data Value
Boost Clinical Trial Data Value
Interactive analysis with GxP compliance
Get more value from your clinical trial data with cohort visualization and analysis tools nested in a GxP-compliant platform that unifies data, bolsters collaboration, and integrates seamlessly into your software suite./cohort-variant-tab.png?width=1280&height=780&name=cohort-variant-tab.png)
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Cohort Analysis and Visualization for Patient/Risk Stratification
Inform patient and risk stratification with powerful cohort analysis and visualization functionality. -
Clinical and Molecular Data Linking
Dive deeper into complex datasets with Spark-backed databases for organizing and linking phenotypic and molecular data. -
IT-ready, GxP-Compliant Data Cloud
Reduce the time and costs associated with building and validating a data management platform. DNAnexus delivers GxP-compliance and industry-leading security that spans from research and development to regulated clinical environments.
Supercharge Collaboration
Supercharge Collaboration
Extensive collaboration and knowledge sharing features
Collaborate with internal and external stakeholders in real-time by sharing projects, data, workflows, and results–all with robust role-based permissioning and comprehensive access controls.
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Secure Data Access for External Teams and Collaborators
Deliver specific datasets and analysis tools to data stakeholders in secure data environments that provide a compliant workspace for external data sharing and research. -
Complete Role-Based Permissioning, Access Controls, and Usage Tracking
Keep your processes secure and funded with comprehensive role-based permission features, guarded data access, and usage and spend reporting. -
Functionality for Real-Time Collaboration and Knowledge Preservation
Iterate in real-time and guard against brain drain with tools that enable project and result sharing, collaborative data analysis, and workflow/protocol cataloging.
Generate Insights
Generate Insights
Powerful tools to inform target and biomarker discovery and development
Go from ingestion to insights with pre-built and custom insight tools that extract more value from your precision health data.
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Longitudinal Analyses and Survival Exploration
Meaningfully interrogate cohort data with tools that visualize patient timelines, model disease trajectories, and provide survival insights. -
Rare Variant Analysis and Report Generation
Quickly go from raw data to rare variant report generation. Easily chain together analytical pipelines for end-to-end, automated insight workflows at production-scale. -
Partnerships that Power Insights
Further explore data through managed partner tools and integrations for biomarker discovery, target discovery, statistical analyses, visualizations, and more.
Customer Stories
Overcoming Technological Challenges to Fast-Track R&D
Discover why Ultragenyx chose to bring data and pipelines together in one secure environment for streamlined multiomics data analysis.
Standardizing Portable, Reproducible Analysis Pipelines
See how Eli Lilly partnered with DNAnexus and used open-source standards to tackle the changing bioinformatics landscape with on-demand compute and portable, reproducible pipelines to run in any region.
Empowering Life Sciences R&D with a Trusted Research Environment
Learn how City of Hope and a top 3 pharma organization partnered with DNAnexus to implement the powerful precision health data environments for management, analysis, and collaboration.
You save the bioinformatician’s time as well as compute time, and therefore decrease turnaround time. This enables R&D researchers to answer questions and get rare disease treatments to market faster. You can’t put a price tag on that.
