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

Publications 6 Datasets 392.5k Experiments 6.2k

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6 matching publication(s)

Publication	Journal	Year	Score	Verdict
Prioritized mass spectrometry increases the depth, sensitivity and data completeness of single-cell proteomics. PMID 37012480	Nat Methods	2023	90	L1 90/100
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs. PMID 36414417	—	2023	85	L1 85/100
GenTB: A user-friendly genome-based predictor for tuberculosis resistance powered by machine learning. PMID 34461978	Genome Med	2021	78	78/100
CRISPR/Cas9 Screens Reveal Multiple Layers of B cell CD40 Regulation. PMID 31365872	Cell Rep	2019	—	L1 No data access
Cell Specific eQTL Analysis without Sorting Cells. PMID 25955312	PLoS Genet	2015	90	L1 90/100
Functional analysis of a duplication (p.E63_D69dup) in the switch II region of HRAS: new aspects of the molecular pathogenesis underlying Costello syndrome. PMID 23335589	—	2013	—	L1 No computation

Prioritized mass spectrometry increases the depth, sensitivity and data completeness of single-cell proteomics.

PMID 37012480 · Nat Methods · 2023

L1 90/100

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.

PMID 36414417 · · 2023

L1 85/100

GenTB: A user-friendly genome-based predictor for tuberculosis resistance powered by machine learning.

PMID 34461978 · Genome Med · 2021

78/100

CRISPR/Cas9 Screens Reveal Multiple Layers of B cell CD40 Regulation.

PMID 31365872 · Cell Rep · 2019

L1 No data access

Cell Specific eQTL Analysis without Sorting Cells.

PMID 25955312 · PLoS Genet · 2015

L1 90/100

Functional analysis of a duplication (p.E63_D69dup) in the switch II region of HRAS: new aspects of the molecular pathogenesis underlying Costello syndrome.

PMID 23335589 · · 2013

L1 No computation