DARE UK Community Groups

We’re supporting new and existing community groups to collaboratively address the needs of the UK sensitive data research community.

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What are DARE UK community groups?

DARE UK community groups are collaborative initiatives co-creating pieces of work that align with the DARE UK vision. Focusing on open communication and knowledge sharing, these groups are working to enhance sensitive data research in the UK.

Setting up or joining a community group

Propose or join new and existing groups to help grow the sensitive data research community. To set up a community group, outline your proposal using the relevant charter template and send it to communities@dareuk.org.uk. To join a community group, visit the community directory and contact the group using the contact information provided. All DARE UK community groups undergo a charter endorsement process and are guided by a code of conduct.

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Community group outputs

DARE UK community groups produce diverse outputs like recommendation documents, open-source software and metadata schema, all assigned a Digital Object Identifier (DOI) and linked to the DARE UK Zenodo community.

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In this presentation, Jo Lam (co-chair of ITALO) introduces a scalable framework for the automated evaluation and benchmarking of data linkage equality, within the NHSE’s new proposed linkage pipeline.

This is from his first milestone presentation at his third week with NHS England PhD Internship Program.  Jo works within the NHS England Data Linkage Hub, lead by Giulia Mantovani (co-chair of ITALO).

As the NHS moves toward a single, authoritative patient record, automated data linkage plays a central role. But without robust evaluation, this process risks embedding systemic biases, especially for marginalised populations. This presentation introduces a transparent, automated framework to benchmark data linkage equality—ensuring linked data are not only accurate, but also fair and trustworthy.

The framework is structured around three interlinked work packages:

  1. Pre-Linkage Profiling:
    Systematic analysis of input data quality—completeness, identifier structure—to assess linkability and detect early bias risks. Outputs include data enrichment reports for owners and linkers to support traceability and audit.
  2. In-Linkage Model Diagnostics:
    Automated tools to evaluate model bias before thresholds are applied. This includes match weight analysis, blocking rule assessment, and interactive bias diagnostics. Enables transparency in strategy selection and allows deviation from a “one-size-fits-all” pipeline when needed.
  3. Post-Linkage Equity Reporting:
    After linkage, sample bias and subgroup-specific error patterns (e.g., by ethnicity or deprivation) are quantified. Outputs include equity dashboards, analyst guidance, and feedback loops to data owners to inform future improvements.

Core assumptions challenged:

  • That all individuals are represented in central systems (e.g., NHS Spine)
  • That input data are equally complete across groups
  • That linked entities reflect ground truth

Key considerations:

  • Trade-offs between precision and recall often mask subgroup disparities.
  • The pipeline must accommodate diverse user needs—data owners, linkers, analysts—while remaining explainable and auditable.

Tools and progress:

  • Synthetic testbeds and reproducible dashboards support open-access benchmarking.
  • Developed in alignment with international best practices (UK, Canada, Australia).
  • Actively integrated with NHS England’s federated linkage infrastructure and informed by the ITALO expert network.

This work delivers practical, automated tooling to detect, explain, and mitigate linkage bias—helping ensure the NHS’s data future is not only powerful, but also inclusive.

ITALO

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