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14 matching publication(s)

Publication	Journal	Year	Score	Verdict
The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases. PMID 28930663	Immunity	2017	67	L1 67/100
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. PMID 22955991	Genome Res	2012	74	L1 74/100
Spatial transcriptomics reveals the molecular signatures of prodromal and advanced α-synucleinopathy. PMID 41736854	iScience	2026	70	L1 70/100
Rfam 15: RNA families database in 2025. PMID 39526405	Nucleic Acids Res	2025	68	L1 68/100
Community assessment of methods to deconvolve cellular composition from bulk gene expression. PMID 39191725	Nat Commun	2024	63	L1 63/100
Transcriptomics, regulatory syntax, and enhancer identification in mesoderm-induced ESCs at single-cell resolution. ⚑ PMID 35977485	Cell Rep	2022	63	L1 63/100 ⚑
A ChIP-exo screen of 887 Protein Capture Reagents Program transcription factor antibodies in human cells. PMID 34426512	Genome Res	2021	57	L1 57/100
Sustainable data analysis with Snakemake. PMID 34035898	F1000Res	2021	71	L1 71/100
Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression. PMID 33722289	Genome Biol	2021	66	L1 66/100
In vivo microscopy reveals macrophage polarization locally promotes coherent microtubule dynamics in migrating cancer cells. PMID 32665556	Nat Commun	2020	50	L1 50/100
Yap1 safeguards mouse embryonic stem cells from excessive apoptosis during differentiation. PMID 30561326	Elife	2018	50	L1 50/100
Viewing RNA-seq data on the entire human genome. PMID 28979763	F1000Res	2017	50	L1 50/100
Spatial organization shapes the turnover of a bacterial transcriptome. PMID 27198188	Elife	2016	71	L1 71/100
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100