Mobiolink
  1. Phase 1 LIS Requests received
  2. 01

    Intake & pre-sorting

    • Systematic processing and classification
    • Intelligent error and exception management
    • Guided pre-processing
    • Dynamic sorting logic and workflow optimization

    Clear steps – less manual work

  3. 02

    Extraction (RNA/DNA)

    • Structured batch generation and control spiking
    • Cycle of sequential process units
    • Provision of measurement-ready eluates

    Secure extraction – fully documented

  4. 03

    PCR setup (plate layout)

    • Strategic consolidation and flexibility (n:n logic)
    • Digital safeguarding and rule verification prior to execution
    • The core USP for PCR laboratories
    • Generation of precise physical operational instructions

    Flexible and controlled – optimal allocation

  5. 04

    Measurement (analyzer)

    • Seamless data import at the analytical device
    • Autonomous execution and optional real-time tracking
    • Structured data export as a trigger for downstream stages

    Clear processes – reliable results

  6. 05

    Automated result interpretation

    • Background ingestion and precise sample mapping
    • Algorithmic curve evaluation and Ct value calculation
    • Comprehensive technical validation
    • Automated release and proactive flagging

    Reliable interpretation – fast and consistent

  7. 06

    Human validation

    • Efficient release matrix and targeted expert focus
    • Interactive curve analysis within the reporting dashboard
    • Complete documentation and audit trail
    • Fully automated LIS ingestion

    Technical validation – focus on what matters

  8. 07

    Export of results to the LIS

    • Quality-driven export barrier and authorization concept
    • Intelligent method mapping and multi-LIS routing
    • Automated code conversion
    • Process transformation in daily laboratory operations

    Results correctly assigned

  9. Phase 2 LIS Validated results exported
Communication with the LIS Process within Mobiolink
02

Extraction (RNA/DNA)

This stage systematically moves individual samples and quality controls into batch-based analysis. Extraction runs manually or automatically through sequential, batch-synchronized process units — through to a measurement-ready eluate.

Structured batch generation and control spiking

Mobiolink manages the assembly of the extraction plate or extraction sequence based on predefined templates. Individual primary samples are precisely combined with all mandatory control samples, standards, blanks, and quality controls into a unified batch. Immediately before the start of the actual extraction, the system supports the precise addition of internal controls (for PCR assays) or internal standards (for analytical chemistry) to each individual sample to ensure seamless analytical monitoring.

Mobiolink interface: layout of a 96-well plate with assays per sample

Cycle of sequential process units

The subsequent extraction process – whether performed manually or managed via automated liquid handling systems – is structured into a sequence of predefined, cyclic process units. The system guides and logs each sub-step, which is executed batch-wise and sequentially across all samples within the run:

  • Precise addition of specific reagents and buffer solutions
  • Temperature-controlled incubation phases
  • Mechanical shaking and mixing workflows
  • Selective washing steps for purification
  • Centrifugation or separation cycles

Provision of measurement-ready eluates

The ultimate output of this coordinated batch run is a homogeneous, purified eluate. System-wide tracking of reagent lots, volumes, and operational steps guarantees that nucleic acids or target analytes remain stable. The resulting eluates are thus flawlessly prepared for the immediate subsequent measurements and the respective molecular or chemical detection techniques.

Next PCR setup (plate layout)