Ingest with provenance
Every source enters with accession, release, licensing context, cohort metadata, and file identity.
REELD workflows are designed to be reconstructed, challenged, and transferred across public datasets.
Every source enters with accession, release, licensing context, cohort metadata, and file identity.
Gene identifiers, cell labels, phenotype terms, and reference builds are mapped with retained ambiguity.
Analyses are built around a named mechanism and its plausible competing explanations.
Genomic, cellular, and phenotype layers remain visible inside one evidence graph.
We vary datasets, parameters, ontology rules, controls, and label resolution.
Code, environment locks, manifests, and limitations travel with every release-ready output.
A result without its analytical context is not portable.
We can help pressure-test a rare-disease analysis before it becomes a mechanistic claim.