Genomics Software Solutions
Genomics Lab Software, Built in Half the Time
Pre-built, production-tested software covers every stage of the lab workflow, from order intake to the clinical report. Each component is customized to a lab's own assays and systems, ships in about half the usual build time, and stays fully owned by the lab.
Engineered for 21 CFR Part 11, HIPAA, and CLIA/CAP environments, and deployed inside yours.
Genomic test turnaround time is a software problem
Sequencing stopped being the slow part years ago. These days the delay in a genomic report comes from the software around the science rather than the science itself, whether that is a requisition being re-keyed manually, an order that failed silently in transit, a pipeline run that died unnoticed overnight, or a finished report waiting in a developer's queue.
That leaves most labs with an unfair choice. Building the software in-house can cost a year of engineering before turnaround improves, and buying a closed platform means handing over control of the data and the classifications that took years to build. There is a better way to close these gaps, and it sits in between.
Genomics software customizable as per your workflow
Each piece of software has already been proven on real clinical lab workflows and comes ready to customize, so a project begins around the halfway mark instead of at zero. Everything runs inside the lab's own environment, and the lab owns it outright once the engagement ends.
The payoff is faster turnaround. Because these components take care of the handoffs between intake, the pipeline, interpretation, and reporting, they remove the exact points where a report tends to stall.
| Build in-house | Buy a closed platform | Start with NonStop.io |
|---|---|---|
| Total control, but a year of engineering and upkeep that never really ends. | Live quickly, though the data, classifications, and audit history stay locked in. | Proven parts, customized to the lab's stack, shipped 40–50% faster, and fully owned by you. |
Deciding between build and buy? It is worth reading Build vs. Buy: Genomics Software in 2026 and the real cost of a clinical genomics platform before deciding.
Software for every stage of the genomics lab workflow
Intake teams re-key hundreds of requisition forms a day across dozens of provider layouts, and a single wrong insurance ID or missing ICD code can travel all the way to billing before it comes back as a denied claim weeks later.
Explore SmartReqA surprising number of EHR orders fail quietly in transit, whether from a malformed HL7 message, a missing segment, or a duplicate retry, and the first sign of trouble is usually a denied claim or a clinic calling to ask where a result has gone.
Explore IntergenixWhen pipelines run across HPC and cloud, there is rarely a single place to see what failed and why, so a run can die overnight and the compute cost stays hidden until the monthly bill arrives.
Explore StrixFlowAnalysts look up every candidate variant in ClinVar, gnomAD, and OMIM and apply ACMG/AMP criteria by hand, which becomes the single largest drain on turnaround time once test volumes grow.
Explore VarionA lab's accumulated clinical judgment is its most valuable asset, yet a closed vendor platform makes that knowledge almost impossible to search, migrate, or build on, and much of it leaves the moment an analyst does.
Explore GENVAREvery new report type or change in regulatory wording tends to need a developer ticket and a months-long wait, and without an approval step in between, an unsigned report can reach a clinician.
Explore ReportStudioWhat clinical labs get back — measured across real engagements
In every engagement, the same result shows up, and it is the one that matters most: hours and weeks of expert time come back to the people doing the science.
| Solution | Impact | Detail |
|---|---|---|
| SmartReq | ~90% intake time eliminated | Under 2 min per form, near-zero entry errors, full audit log |
| Intergenix | ~80% integration effort cut | Zero manual re-entry, 8–12 hrs/week saved |
| StrixFlow | ~60% ops cost saved | 4–8 hrs/day of debugging recovered, full cost visibility |
| Varion | ~80% time-to-report saved | Review time to 30–60 minutes per case |
| GENVAR | ~60% re-work eliminated | Under 2 min to surface variant evidence |
| ReportStudio | ~90% report cycle time saved | Report changes in 1–2 weeks, owned by lab staff |
* Impact figures are NonStop.io estimates and vary by engagement scope.
How we build genomics software with your team
On-premise or cloud
Every component can be self-hosted, so PHI and genomic data never leave the lab's environment.
Fits your stack
It connects over HL7/FHIR and Mirth Connect to the LIMS and EHR a lab already runs, rather than replacing them.
Compliance-first
Audit logging, role-based access, and traceability are engineered in for 21 CFR Part 11, HIPAA, and ISO 27001 from the very start.
Weeks, not quarters
Engagements are fixed in scope and delivered with IQ/OQ/PQ validation artifacts, so there is never an open-ended retainer.
Built for clinical diagnostics and genetic testing labs
Clinical diagnostics and genetic testing labs scaling volumes under CAP/CLIA pressure
Precision medicine companies building proprietary interpretation and AI on their own data
Genomics and biotech teams modernizing pipelines, interoperability, and reporting without a full rebuild
Frequently Asked Questions
Are these off-the-shelf products?
How much development time does this save?
Will it connect to our existing LIMS, EHR, and pipelines?
How do you reduce turnaround time in a genetics lab?
Is on-premise better for PHI?
Do labs have to adopt all six?
Book a call
Find the gap worth closing first
Book a 15-minute scoping call. We will map your current stack together, point to where the software fits, and tell you plainly if it does not.
Book a call →