Current release: CoGenEx-PM3

GLEAM-DB

Genomic Literature Evidence Atlas Map

GLEAM-DB provides auditable literature-derived evidence records for variant interpretation. The first release, CoGenEx-PM3 (Co-occurring Genotype Evidence eXtractor for PM3 allelic-configuration evidence), focuses on PM3 allelic-configuration evidence and links genetic variants to PMID-level evidence records extracted from primary articles and supplementary materials.

Examples:

Supported high-confidence inputs in this portal release: NM:c.HGVS, Gene:c.HGVS, and c.HGVS.

Release versionv1.0
Audit unitPMID x variant
Candidate PMIDs17637
PMID × variant records103889
Full-text available PMIDs17435
Unique genes1281
Unique variants48289
PM3-positive records3842

Resource statement

GLEAM-DB is not a final clinical classification system. It provides literature-derived PM3 evidence records to support evidence review, curation, benchmarking and reproducible variant interpretation.