INTEGRATED PARTNER|intoDNA Technology

    STRIDE® IntegrationNative on BioCompute

    The first platform technology for direct, sensitive detection and quantification of DNA breaks at the individual lesion level. Unlike conventional methods dependent on complex DDR signaling, STRIDE® provides proximal, quantifiable readouts with single-lesion sensitivity.

    What Makes STRIDE® Different?

    Breakthrough technology enabling direct DNA damage detection without reliance on cellular signaling pathways.

    Single-Lesion Sensitivity

    Detect and quantify DNA breaks at the individual lesion level—no reliance on complex DDR signaling pathways.

    DDR Inhibitor Validation

    Validate targets and mechanism-of-action studies with direct, quantifiable readouts.

    PD Biomarker Development

    Develop pharmacodynamic biomarkers for clinical trials with unprecedented precision.

    Pathway Analysis

    Functional analysis of HR, MMR, and BER pathways with visual evidence.

    BioCompute + STRIDE®

    Native Integration Benefits

    STRIDE® runs natively on the BioCompute platform, ensuring your DNA damage data flows seamlessly through our Evidence Engine with full regulatory compliance.

    • Native integration with BioCompute Evidence Engine
    • Automated audit trails for FDA 21 CFR Part 11 compliance
    • Single-cell resolution data ingestion
    • Real-time quantification with sovereign compute
    • AstraZeneca-validated DDR analysis workflows
    • Visual evidence generation for regulatory submissions

    STRIDE® Workflow

    Integrated Analysis Pipeline

    1

    Sample Ingestion

    Single-cell resolution data capture

    2

    STRIDE® Analysis

    DNA break quantification

    3

    Evidence Generation

    Audit-ready visual reports

    4

    Regulatory Export

    FDA 21 CFR Part 11 compliant

    Use Cases

    How leading pharma and biotech companies leverage STRIDE® on BioCompute.

    90%

    faster target validation

    Oncology Drug Development

    Validate DDR-targeting compounds with single-molecule precision. Fail fast on ineffective candidates before costly clinical trials.

    21 CFR

    Part 11 compliant

    Radiopharmaceuticals

    Quantify DNA damage from radiolabeled compounds with audit-ready evidence for IND submissions.

    100%

    traceability

    Genome Editing Safety

    Assess off-target effects and genotoxicity with visual evidence at single-cell resolution.

    Ready to Experience STRIDE®?

    Join leading pharma and biotech companies using STRIDE® on BioCompute for FDA-ready DNA damage analysis.