Gather the context
Connect run, sample, study, and publication records across public sources.
reOmics is developing auditable metadata for human RNA-seq. The first milestone is a validated cohort table, designed to support future search and targeted expression and splicing evidence for drug-development research.
Sequencing files are abundant. The details that make them useful can be scattered across records, buried in free text, or absent altogether.
Before researchers can compare samples, they need to know which tissue, disease, subject, treatment, and experiment each sample represents.
See the data challengereOmics starts with auditable metadata curation. Search and prioritized processing are planned stages built on that foundation.
Connect run, sample, study, and publication records across public sources.
Extract and normalize tissue, disease, assay, and cohort descriptors with a reviewable evidence trail.
Use curated cohorts to guide search and prioritize deeper expression and splicing analysis.
reOmics aims to turn fragmented descriptions into structured fields, with source links, confidence, and review status attached to the record.
How the platform is plannedTissue · disease · cell type · phenotype
Donor · case/control · treatment · timepoint
Assay · layout · run · sample · study
Publication · provenance · review status · confidence
Members of the reOmics team contributed to the recount ecosystem. Its published work shows the scale of the processing foundation; reOmics is a separate, developing effort.
Historical recount3 figures, not reOmics platform totals. Wilks et al., Genome Biology (2021) ↗
Find relevant public studies across tissue, disease, assay, and experimental context.
Bring comparable expression and splicing evidence to early target questions.
Explore exon and splice-site evidence in cohorts relevant to RNA-directed strategies.
Study disease-associated transcriptomic patterns with clearer cohort definitions.
The pitch deck outlines a staged model: make metadata useful and correctable, then develop query access and partner-specific evidence around selected cohorts. These are planned offerings.
Publish curated tables, schemas, and correction workflows to make cohort definitions easier to inspect and improve.
Develop access to disease, tissue, and assay cohorts with provenance and confidence for research teams.
Prioritize processing and partner-specific expression or splicing evidence around defined research questions.
We welcome conversations about public RNA-seq cohorts, transcriptomic evidence, and research partnerships.