Corpus 1,278 assessed · 1,179 scored · 644 reproduced ≥75 · 170 flagged ·∅ 74/100

Publications 303 Datasets 392.5k Experiments 4.9k

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303 matching publication(s)

Publication	Journal	Year	Score	Verdict
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. PMID 17033964	—	2006	75	L1 75/100
Long-read nanopore shotgun metagenomic DNA sequencing for river biodiversity, wildlife, pollution, and environmental health monitoring. PMID 42038409	NAR Genom Bioinform	2026	78	L1 78/100
nf-core/mag: a best-practice pipeline for metagenome hybrid assembly and binning. PMID 35118380	NAR Genom Bioinform	2022	100	L1 100/100

Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.

PMID 17033964 · · 2006

L1 75/100

Long-read nanopore shotgun metagenomic DNA sequencing for river biodiversity, wildlife, pollution, and environmental health monitoring.

PMID 42038409 · NAR Genom Bioinform · 2026

L1 78/100

nf-core/mag: a best-practice pipeline for metagenome hybrid assembly and binning.

PMID 35118380 · NAR Genom Bioinform · 2022

L1 100/100