You need genetic analyses for a research project, a study or a collaboration but don't want to build your own high-throughput lab? Novogenia is your lab service for research: SNP genotyping, sequencing and sample processing in our own, certified EU genetic lab — reproducible and scalable.
Targeted genotyping of defined markers for your study — precise, reproducible and at high throughput for large cohorts.
Sequencing of selected regions as a basis for your research questions — cleanly prepared and documented.
Preparation, extraction and quality control of the sample material as a reliable basis for every further analysis.
Clear registration, storage and tracking of the study samples — seamless traceability across the entire project.
Results as structured raw data in the format your statistical evaluation or pipeline requires.
From a pilot cohort to a large study population — we scale the processing together with your study design.
Your study samples are processed in our own EU genetic lab — not passed on anonymously, but analyzed under clear responsibility.
More than 30 self-developed genetic tests and over 15 years of lab practice stand behind every genotyping and sequencing run.
Automated workflows allow large sample numbers to be processed at consistent quality — important for meaningful studies.
Standardized processes and quality control ensure reproducible results on which dependable research can be built.
Clear assignment and tracking of every sample guarantee data integrity across the entire research project.
Whether a one-off contract analysis, a project-accompanying lab service or methodological cooperation — we adapt to your study design.
Research projects often face the same bottleneck: the research question is clear, but the lab capacity for a larger cohort is missing. Novogenia provides it — with SNP genotyping, sequencing and high-throughput processing in our own EU genetic lab. You deliver study design and samples, we deliver reproducible raw data in the format your evaluation needs. That way your energy stays on the research, not on running a lab.
Discuss your study →Not every research institution has its own high-throughput genetic lab — and building one isn't worthwhile for many projects. Instruments, maintenance and qualified staff tie up funds that, in many studies, are better spent on the actual research.
An external lab service is then the more efficient route: you hand the genotyping or sequencing to a specialized genetic lab and focus on study design, research question and evaluation. Novogenia operates its own, certified EU genetic lab in Salzburg and has been active since 2009. That gives you lab capacity on demand, without investing long-term in infrastructure that sits unused after the project ends.
SNP genotyping is the method of choice in many studies when defined genetic markers are to be determined across a large cohort. It is efficient, easy to standardize and particularly suitable when the variants under investigation are already known.
What's decisive here are reproducibility and consistent quality across all samples — otherwise the statistical power of the study suffers. Standardized workflows and continuous quality control ensure that your genotyping data remains dependable, even with large sample numbers. If data quality fluctuates between individual runs, it can hardly be repaired in the later evaluation — which is why good research begins with reliable lab work.
Where genotyping queries defined markers, sequencing opens up a more detailed view of selected genetic regions. For research projects that go beyond known markers or aim to discover new variants, it delivers the necessary depth.
What matters is clean sample preparation and end-to-end documentation, so that the data produced fits your evaluation and pipeline. Which approach is right for your study — targeted genotyping or sequencing — depends on your research question, the cohort size and the budget. We're happy to clarify together which method supports your research goal most efficiently.
Meaningful studies often need many samples — and therefore a lab that scales. Automated high-throughput processes allow large cohorts to be processed at consistent quality, which would hardly be achievable with manual processing.
At Novogenia you can start with a pilot cohort and then scale up the sample processing without reproducibility of the data suffering. That way the lab capacity grows together with your study design — whether you first run a small feasibility study or directly analyze a large population. Throughput never comes at the expense of consistency: every sample goes through the same standardized process.
In research, data integrity is non-negotiable. Every study sample must be clearly assigned, registered and traceable — from sample intake through quality control to analysis.
Seamless sample management prevents mix-ups and ensures that your results can always be traced back to the right sample. That is the foundation for reproducible and verifiable research — and it protects your study from exactly the errors that can no longer be corrected afterwards. A swapped or mislabeled sample can invalidate an entire evaluation; clean sample management is therefore not a detail but a foundation.
Genetic raw data is only useful if it fits your evaluation. That's why we deliver the results in the format your statistical analysis or pipeline requires — as structured raw data for further processing.
The evaluation and interpretation remain with you and your research team, while we secure the reliable data foundation in the lab. This clear division of labor makes particular sense in science: you retain full control over analysis and conclusions but hand the resource-intensive lab work to an experienced partner. That keeps scientific interpretive authority where it belongs, while data quality is secured in the lab. At the start, we agree together which formats, annotations and identifiers your pipeline expects, so that the delivered raw data flows into your evaluation without rework.
Research projects differ greatly in scope, duration and budget — so the collaboration with a lab should be just as flexible. Some projects only need a one-off contract analysis of a completed cohort, others a project-accompanying lab service that runs across several phases and sample intakes.
Novogenia tailors the model to your study design. You can start with a small feasibility study and, if things go well, seamlessly scale up to the large main cohort without changing lab partners. For multi-phase studies, seamless sample management ensures that samples from different time points are processed consistently and remain comparable. That gives you lab capacity oriented around your scientific roadmap — not the other way around.
Novogenia combines its own, certified EU genetic lab with over 15 years of lab experience and more than 30 self-developed genetic tests. For research projects and universities this means: SNP genotyping, sequencing and sample management from a single source, with reproducible data and scalable capacity.
Whether a one-off contract analysis or a project-accompanying lab service across several study phases — we adapt to your study design and your timeline. You gain a lab partner that understands the methodological demands of research and delivers reliable data on which dependable findings can be built. Submit your research inquiry now or ask our AI assistant directly.
Tell us about your research project — we'll get back to you with the method, throughput and timeline for your cohort. Or ask our AI assistant directly, around the clock.