Time-to-answer stalls after sequencing.
Data can move quickly, but reporting, review, triage, and escalation often remain manual or unclear.
For commercial, centralized, and reference labs
Theiagen helps labs turn pathogen sequencing capacity into validated workflows, interpretable outputs, and scalable services that customers can actually use.
The bottleneck
The hard part is moving from isolated sequencing runs to reliable service lines that laboratory leaders, scientific directors, commercial teams, and customers can trust.
Data can move quickly, but reporting, review, triage, and escalation often remain manual or unclear.
New assays need reproducible analysis, versioned workflows, defensible QC, and clear evidence trails.
Hospital systems, infection prevention, pharma, food, and public-sector buyers need outputs built for decisions.
Bioinformatics expertise is difficult to hire, retain, and standardize across a growing test menu.
Commercial lab operating layer
Theiagen brings pathogen-specific bioinformatics, training, workflow design, and support into a launch model that can be validated, explained, and transferred into lab operations.
Taxon-aware pipelines, QC structure, metadata requirements, run review patterns, and versioned implementation plans.
Training for scientific, technical, and commercial teams so outputs are understood and used consistently.
Review workflows, troubleshooting, reporting patterns, and customer-facing launch support for new service lines.
Fixed-scope pilots
Each pilot is designed to produce usable proof artifacts: workflow map, validation considerations, sample output, operating requirements, and a launch recommendation.
Evaluate how sequencing and relatedness analysis can support outbreak investigation, infection prevention, and customer-facing reporting.
Turn genomic and resistance context into a structured intelligence product for infection prevention, stewardship, and lab customers.
Plan a service line from workflow and validation through reporting, training, sales enablement, and launch support.
Launch support
A commercial launch needs more than a pipeline. Theiagen helps teams define what the lab will sell, how it will be validated, what customers will receive, and how internal teams will support it.
Stakeholder value
Launch credible pathogen-genomics services without building every workflow, report, and support process from scratch.
Use reproducible, explainable workflows with clearer evidence trails and review expectations.
Bring a concrete service story to customers with example outputs, implementation scope, and practical use cases.
Receive pathogen-genomics outputs that are structured for infection prevention, surveillance, stewardship, or operational decisions.
Pathogen-genomics expertise
Theiagen's public work spans multi-laboratory implementations, international bioinformatics enablement, and practical training programs in public health genomics. The commercial lab offer brings that workflow, training, and support discipline into focused service-line launches.
Pilot process
Pick the commercial opportunity, target customer, and operational constraints.
Map inputs, metadata, pipelines, QC gates, review, and output requirements.
Run representative analysis or workflow evaluation within the pilot scope.
Produce a sample report structure, technical appendix, and workflow evidence map.
Review feasibility, validation path, staffing, customer fit, and next-step roadmap.
Sample output package
The pilot produces tangible outputs your team can review, refine, and use in customer conversations as the service moves toward launch.
Plain-language finding categories, action context, uncertainty notes, and recommended escalation patterns.
QC, pipeline versioning, metadata, analytical notes, and review checkpoints for scientific teams.
Handoffs, staffing expectations, review model, validation considerations, and launch-readiness gaps.
Resources
A practical view of where pathogen genomics can create defensible commercial services.
Open resourceA concise overview for leadership, business development, and scientific stakeholders.
Open resourceKey questions for workflow versioning, QC, review, metadata, and documentation.
Open resourceA practical frame for evaluating customer fit, operating requirements, and next steps.
Open resourceFAQ
No. Theiagen is focused on bioinformatics, workflow implementation, reporting structure, validation support, training, and operational launch support.
Yes. The pilot begins by mapping current instrumentation, sample types, metadata, operational constraints, and reporting needs before recommending the implementation path.
Yes. The fixed-scope pilot is designed to help leadership evaluate feasibility, customer value, validation scope, and operating requirements before broader rollout.
Potential users include hospital systems, infection prevention teams, public health partners, pharma or biotech teams, food safety organizations, and other customers that need pathogen-genomics intelligence.
Theiagen avoids unsupported claims. Pilot outputs are structured around reproducible workflows, evidence trails, clear limitations, and the lab's validation and review framework.
Pick one commercial use case, one pilot question, and the internal stakeholders who need to approve a launch decision. Theiagen can help shape the scope from there.
Start the conversation
Tell us which pathogen-genomics service you want to bring to market first. We will help shape a pilot with clear outputs, review points, and launch-ready next steps.
Your team is evaluating a pathogen-genomics service line, needs validation-aware implementation support, or wants customer-ready output examples for a commercial pilot.