Powerful software for automated qPCR data analysis
Replace fragmented qPCR analysis workflows with one platform
1. Import raw run data
Automatically collect and import raw data from supported qPCR instruments.
2. Analyse with assay-specific logic
Apply predefined thresholds, controls, and multiplex interpretation rules.
3. Review and approve results
Flag exceptions, comment, re-analyse if needed, and approve results with full traceability.
4. Export and integrate
Send standardized results to LIS/LIMS or export in a structured PDF report.
Core capabilities
GeneBlink provides a complete platform for automated qPCR data analysis and interpretation.
- Automated data analysis
- Standardized interpretation
- Workflow, review & reporting
- Integration, compliance & control
Automated analysis from raw qPCR data
GeneBlink automatically processes raw qPCR data, eliminating manual threshold setting and reducing variability across runs and instruments.
- Amplification and melt curve analysis
- Absolute quantification
- Multi-level data exploration (run, plate, well)
- Re-analysis with updated parameters
Assay-specific interpretation, applied consistently
GeneBlink applies predefined interpretation logic tailored to each assay, ensuring consistent results across instruments, users, and laboratories.
- Ct/Cq thresholds and interpretation ranges
- Result classification (positive / negative / inconclusive)
- Multiplex panel logic
- Control evaluation and reflex testing rules
Structured workflows for validation and reporting
GeneBlink enables controlled review, approval, and reporting of results within a single environment, replacing fragmented manual processes.
- Visualization and flagged result review
- Review and approval workflows
- Commenting and audit-ready traceability
- PDF and CSV result export
Seamless integration with full traceability
GeneBlink connects instruments and laboratory systems while ensuring secure, compliant, and fully traceable workflows.
- Automatic import from qPCR instruments
- LIS/LIMS integration
- Role-based access control
- Audit trails and electronic signatures
- Support for IVDR and 21 CFR Part 11 workflows
Automated data analysis
Automated analysis from raw qPCR data
GeneBlink automatically processes raw qPCR data, eliminating manual threshold setting and reducing variability across runs and instruments.
- Amplification and melt curve analysis
- Absolute quantification
- Multi-level data exploration (run, plate, well)
- Re-analysis with updated parameters
Standardized interpretation
Assay-specific interpretation, applied consistently
GeneBlink applies predefined interpretation logic tailored to each assay, ensuring consistent results across instruments, users, and laboratories.
- Ct/Cq thresholds and interpretation ranges
- Result classification (positive / negative / inconclusive)
- Multiplex panel logic
- Control evaluation and reflex testing rules
Workflow, review & reporting
Structured workflows for validation and reporting
GeneBlink enables controlled review, approval, and reporting of results within a single environment, replacing fragmented manual processes.
- Visualization and flagged result review
- Review and approval workflows
- Commenting and audit-ready traceability
- PDF and CSV result export
Integration, compliance & control
Seamless integration with full traceability
GeneBlink connects instruments and laboratory systems while ensuring secure, compliant, and fully traceable workflows.
- Automatic import from qPCR instruments
- LIS/LIMS integration
- Role-based access control
- Audit trails and electronic signatures
- Support for IVDR and 21 CFR Part 11 workflows
Perfect fit into your existing laboratory ecosystem
GeneBlink integrates into your existing workflow without replacing your instruments or laboratory systems, connecting previously fragmented steps into one streamlined and standardized workflow.
WITHOUT GENEBLINK
✔ Instrument-dependent software
✔ Manual threshold adjustment
✔ Excel-based interpretation
✔ Manual reporting
WITH GENEBLINK
✔ Automatic data import from qPCR instruments
✔ Automated analysis and interpretation
✔ Structured review and approval
✔ Direct export to LIS/LIMS or reports
Designed for real diagnostic workflows
GeneBlink centralizes amplification curve visualization, multilevel result review, workflow approval, and reporting in one software environment. Teams can move from completed run to validated output with less manual effort and greater consistency.
Explore how GeneBlink fits your workflow
See how GeneBlink can standardize your qPCR analysis across instruments, assays, and teams.
Fast implementation and seamless integration
GeneBlink is designed for quick deployment within existing laboratory environments, minimizing IT workload and allowing your team to focus on analysis, not setup.
Our team supports integration with your qPCR instruments and laboratory information systems, ensuring a smooth flow of data from analysis to reporting. We also provide the documentation required for validation, helping you align with regulatory and internal quality requirements from the start.
STANDALONE SOFTWARE
- Ready-to-use platform for laboratories
- Configured to your assays, workflows, and systems
OEM / WHITE-LABEL DEPLOYMENT
- Custom branding (UI, reports, workflows)
- Kit-specific interpretation logic
- Branded outputs and user experience
AUTOMATION AND PLATFORM INTEGRATION
- Analysis engine for end-to-end diagnostic systems
- Integration into instrument and workflow software
Flexible deployment and OEM options
GeneBlink is configured to match your operational structure, workflow complexity, and regulatory requirements.
It can be deployed as a standalone platform or integrated into your own diagnostic solution.
Whether you operate a single laboratory, develop diagnostic kits, or build integrated systems, the platform can be tailored to your use case, from focused analysis workflows to fully customized, integrated solutions.
For partners, the platform is available as a fully customizable white-label solution, enabling you to embed GeneBlink directly into your product offering.
Ongoing support & maintenance
Our team supports you through implementation and validation within your existing environment, ensuring a seamless start and full regulatory alignment.
You’ll also receive continuous support and maintenance from our development team, keeping GeneBlink secure, reliable, and always up to date.
FAQ
Choosing new qPCR data analysis software comes with many considerations. Below are some of the most common questions we receive about GeneBlink and its capabilities.
If you have any other questions, our team is happy to help. Contact us at team@biosistemika.com to discuss your specific needs or request additional information about GeneBlink.
Is GeneBlink compatible with my qPCR instrument?
Yes. GeneBlink supports data import from major qPCR instruments and file formats used by leading diagnostic platforms. If your instrument isn’t listed, our team can easily configure compatibility through a custom integration or file parser.
Can I use GeneBlink for regulated diagnostic workflows (IVD/IVDR)?
Absolutely. GeneBlink was designed for regulated environments, featuring audit trails, user authentication, electronic signatures, and documentation aligned with IVDR and 21 CFR Part 11 requirements.
How is GeneBlink different from other qPCR data analysis software?
Unlike generic data analysis tools, GeneBlink combines automation, flexibility, and compliance in one platform. It adapts to your assays and logic, provides complete visibility into amplification and melting curve quality, and integrates directly with your reporting workflows.
Ready to streamline your qPCR analysis?
Explore how GeneBlink can support your qPCR workflows.