Corpus 1,285 assessed · 1,186 scored · 647 reproduced ≥75 · 174 flagged ·∅ 73.9/100

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1 matching publication(s)

Publication	Journal	Year	Score	Verdict
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflow. PMID 41685349	NAR Genom Bioinform	2026	—	L1 No data access

Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflow.

PMID 41685349 · NAR Genom Bioinform · 2026

L1 No data access