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

Publications 3 Datasets 392.5k Experiments 4.7k

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3 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
Automatic discovery of 100-miRNA signature for cancer classification using ensemble feature selection. PMID 31533612	BMC Bioinformatics	2019	69	L1 69/100
Nimbus: a design-driven analyses suite for amplicon-based NGS data. PMID 29538618	Bioinformatics	2018	64	L1 64/100

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

Automatic discovery of 100-miRNA signature for cancer classification using ensemble feature selection.

PMID 31533612 · BMC Bioinformatics · 2019

L1 69/100

Nimbus: a design-driven analyses suite for amplicon-based NGS data.

PMID 29538618 · Bioinformatics · 2018

L1 64/100