Corpus 1,272 assessed · 1,173 scored · 643 reproduced ≥75 · 168 flagged ·∅ 74.1/100

Publications 1 Datasets 392.5k Experiments 4.7k

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Filters: 2026 ✕ Computer science ✕ udn rare disease patients (144 patients / 165 samples) ✕ clear all

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