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18 matching publication(s)

Publication	Journal	Year	Score	Verdict
Rfam 15: RNA families database in 2025. PMID 39526405	Nucleic Acids Res	2025	68	L1 68/100
Interpretable prediction models for widespread m6A RNA modification across cell lines and tissues. PMID 37995291	Bioinformatics	2023	79	L1 79/100
Graph Random Forest: A Graph Embedded Algorithm for Identifying Highly Connected Important Features. PMID 37509188	Biomolecules	2023	89	L1 89/100
treeclimbR pinpoints the data-dependent resolution of hierarchical hypotheses. PMID 34001188	Genome Biol	2021	73	L1 73/100
TSUNAMI: Translational Bioinformatics Tool Suite for Network Analysis and Mining. PMID 33705981	Genomics Proteomics Bioinformatics	2021	79	L1 79/100
Curation of over 10 000 transcriptomic studies to enable data reuse. PMID 33599246	Database (Oxford)	2021	80	L1 80/100
Omics Playground: a comprehensive self-service platform for visualization, analytics and exploration of Big Omics Data. PMID 33575569	NAR Genom Bioinform	2019	61	L1 61/100
Colorectal Cancer Prediction Based on Weighted Gene Co-Expression Network Analysis and Variational Auto-Encoder. ⚑ PMID 32825264	Biomolecules	2020	80	L1 80/100 ⚑
MasterOfPores: A Workflow for the Analysis of Oxford Nanopore Direct RNA Sequencing Datasets. PMID 32256520	Front Genet	2020	50	L1 50/100
Integrative network modeling reveals mechanisms underlying T cell exhaustion. PMID 32024856	Sci Rep	2020	59	L1 59/100
A Bayesian approach to accurate and robust signature detection on LINCS L1000 data. PMID 32003771	Bioinformatics	2020	37	L1 37/100
Automatic discovery of 100-miRNA signature for cancer classification using ensemble feature selection. PMID 31533612	BMC Bioinformatics	2019	69	L1 69/100
SMAC, a computational system to link literature, biomedical and expression data. PMID 31324861	Sci Rep	2019	50	L1 50/100
pysradb: A Python package to query next-generation sequencing metadata and data from NCBI Sequence Read Archive. PMID 31114675	F1000Res	2019	90	L1 90/100
pwrEWAS: a user-friendly tool for comprehensive power estimation for epigenome wide association studies (EWAS). PMID 31035919	BMC Bioinformatics	2019	88	L1 88/100
miRge 2.0 for comprehensive analysis of microRNA sequencing data. PMID 30153801	BMC Bioinformatics	2018	89	L1 89/100
Easy and efficient ensemble gene set testing with EGSEA. PMID 29333246	F1000Res	2017	97	L1 97/100
A robust data scaling algorithm to improve classification accuracies in biomedical data. PMID 27612635	BMC Bioinformatics	2016	87	87/100