Publications 25 Datasets 392.5k Experiments 4.7k

Explore

25 matching publication(s)

Publication	Journal	Year	Score	Verdict
A single-cell survey of Drosophila blood. PMID 32396065	Elife	2020	94	L1 94/100
Protocol for transcriptomic and epigenomic analysis of JAK inhibitor sensitivity in IFN-γ-primed human macrophages using ATAC-seq and RNA-seq. PMID 41313685	STAR Protoc	2025	85	L1 85/100
Smart spatial omics (S2-omics) optimizes region of interest selection to capture molecular heterogeneity in diverse tissues. PMID 41298871	Nat Cell Biol	2025	100	L1 100/100
Distinct senotypes in p16- and p21-positive cells across human and mouse aging tissues. PMID 41162753	EMBO J	2025	50	L1 50/100
Tumor-specific but immunosuppressive CD39+CD8+ T cells exhibit double-faceted roles in clear cell renal cell carci PMID 40961944	Cell Rep Med	2025	88	L1 88/100
Integrative analysis of single-cell RNA-seq and gut microbiome metabarcoding data elucidates macrophage dysfunction in mice with DSS-induced ulcerative colitis. PMID 38879692	Commun Biol	2024	69	L1 69/100
VirPipe: an easy-to-use and customizable pipeline for detecting viral genomes from Nanopore sequencing. PMID 37129547	Bioinformatics	2023	83	L1 83/100
Hierarchical cell-type identifier accurately distinguishes immune-cell subtypes enabling precise profiling of tissue microenvironment with single-cell RNA-seque PMID 36681937	Brief Bioinform	2023	94	L1 94/100
Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data. PMID 36295018	Life (Basel)	2022	—	L1 No computation
msPIPE: a pipeline for the analysis and visualization of whole-genome bisulfite sequencing data. PMID 36123620	BMC Bioinformatics	2022	100	L1 100/100
Assessment of genotyping array performance for genome-wide association studies and imputation in African cattle. PMID 36057548	Genet Sel Evol	2022	90	L1 90/100
Bioinformatics Strategies to Identify Shared Molecular Biomarkers That Link Ischemic Stroke and Moyamoya Disease with Glioblastoma. ⚑ PMID 36015199	Pharmaceutics	2022	19	L1 19/100 ⚑
Base editing in human cells with monomeric DddA-TALE fusion deaminases. PMID 35821233	Nat Commun	2022	95	L1 95/100
Enhancer RNAs stimulate Pol II pause release by harnessing multivalent interactions to NELF. PMID 35508485	Nat Commun	2022	55	L1 55/100
Effect of PAIP1 on the metastatic potential and prognostic significance in oral squamous cell carcinoma. ⚑ PMID 35153296	Int J Oral Sci	2022	10	L1 10/100 ⚑
Expression of neurofibromin 1 in colorectal cancer and cetuximab resistance. PMID 34779495	Oncol Rep	2021	73	L1 73/100
Computationally scalable regression modeling for ultrahigh-dimensional omics data with ParProx. PMID 34254998	Brief Bioinform	2021	79	L1 79/100
Collisionless relaxation of a disequilibrated current sheet and implications for bifurcated structures. PMID 34145266	Nat Commun	2021	95	L1 95/100
Prediction of Alzheimer's disease-specific phospholipase c gamma-1 SNV by deep learning-based approach for high-throughput screening. PMID 33397809	Proc Natl Acad Sci U S A	2021	48	L1 48/100
Prediction of prognostic signatures in triple-negative breast cancer based on the differential expression analysis via NanoString nCounter immune panel. PMID 33138797	BMC Cancer	2020	72	L1 72/100
Wx: a neural network-based feature selection algorithm for transcriptomic data. PMID 31324856	Sci Rep	2019	50	L1 50/100
Whole genome and transcriptome maps of the entirely black native Korean chicken breed Yeonsan Ogye. PMID 30010758	Gigascience	2018	91	L1 91/100
Octopus-toolkit: a workflow to automate mining of public epigenomic and transcriptomic next-generation sequencing data. PMID 29420797	Nucleic Acids Res	2018	68	L1 68/100
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