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

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5 matching publication(s)

Publication	Journal	Year	Score	Verdict
Single duplex DNA sequencing with CODEC detects mutations with high sensitivity. PMID 37106072	Nat Genet	2023	78	L1 78/100
A scalable, open-source implementation of a large-scale mechanistic model for single cell proliferation and death signaling. PMID 35729113	Nat Commun	2022	84	L1 84/100
GEMmaker: process massive RNA-seq datasets on heterogeneous computational infrastructure. PMID 35501696	BMC Bioinformatics	2022	67	L1 67/100
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 20887964	—	2010	—	L1 No computation
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100

Single duplex DNA sequencing with CODEC detects mutations with high sensitivity.

PMID 37106072 · Nat Genet · 2023

L1 78/100

A scalable, open-source implementation of a large-scale mechanistic model for single cell proliferation and death signaling.

PMID 35729113 · Nat Commun · 2022

L1 84/100

GEMmaker: process massive RNA-seq datasets on heterogeneous computational infrastructure.

PMID 35501696 · BMC Bioinformatics · 2022

L1 67/100

WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

PMID 20887964 · · 2010

L1 No computation

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

PMID 18834967 · · 2008

L1 70/100