Genomic references
Population variation, gene constraint, transcript consequences, and disease association resources.
Public data, with its history intact.
We preserve where data came from, what changed, and where reuse should stop.
The source is part of the result.
Cohort design, reference version, tissue handling, and access terms remain attached to every derived object.
Single-cell atlases
Public tissue, organoid, developmental, and disease references with donor-aware analysis.
Phenotype knowledge
Human Phenotype Ontology and disease-gene resources with explicit release tracking.
Functional context
Pathway, interaction, perturbation, and expression resources used as supporting evidence.
Data stewardship
Minimum necessary use
We use only the fields and resolution required for the research question.
Source-aligned terms
Licenses, controlled-access conditions, and attribution requirements travel downstream.
No re-identification
REELD does not attempt to identify participants in public or controlled datasets.
Careful communication
Results are framed to avoid stigmatizing populations or overstating clinical meaning.
Useful public resources
Examples of the infrastructure our field relies on. Resource use depends on each source's current terms.