OOIR: Observatory of International Research

Papers

(The H4-Index of Briefings in Bioinformatics is 71. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-05-01 to 2025-05-01.)

Article	Citations
Cox-Sage: enhancing Cox proportional hazards model with interpretable graph neural networks for cancer prognosis	1000
Corrigendum to: Computational design of ultrashort peptide inhibitors of the receptor-binding domain of the SARS-CoV-2 S protein	467
Knowledge bases and software support for variant interpretation in precision oncology	318
Analysis of super-enhancer using machine learning and its application to medical biology	246
Computational model for ncRNA research	208
COWID: an efficient cloud-based genomics workflow for scalable identification of SARS-COV-2	205
Clustering scRNA-seq data with the cross-view collaborative information fusion strategy	196
Letter regarding article named ‘Is acupuncture effective in the treatment of COVID-19 related symptoms? Based on bioinformatics/network topology strategy’	189
DeepCheck: multitask learning aids in assessing microbial genome quality	188
GAABind: a geometry-aware attention-based network for accurate protein–ligand binding pose and binding affinity prediction	173
Balancing the transcriptome: leveraging sample similarity to improve measures of gene specificity	171
Genome sequencing data analysis for rare disease gene discovery	169
CharID: a two-step model for universal prediction of interactions between chromatin accessible regions	164
Defining the functional divergence of orthologous genes between human and mouse in the context of miRNA regulation	161
ETLD: an encoder-transformation layer-decoder architecture for protein contact and mutation effects prediction	156
CLT-seq as a universal homopolymer-sequencing concept reveals poly(A)-tail-tuned ncRNA regulation	153
Combining power of different methods to detect associations in large data sets	147
SGNNMD: signed graph neural network for predicting deregulation types of miRNA-disease associations	142
Novel multi-omics deconfounding variational autoencoders can obtain meaningful disease subtyping	140
Clustered tree regression to learn protein energy change with mutated amino acid	133
Blood-based transcriptomic signature panel identification for cancer diagnosis: benchmarking of feature extraction methods	131
SCSMD: Single Cell Consistent Clustering based on Spectral Matrix Decomposition	123
Attribute-guided prototype network for few-shot molecular property prediction	120
A multichannel graph neural network based on multisimilarity modality hypergraph contrastive learning for predicting unknown types of cancer biomarkers	118
Ensemble classification based feature selection: a case of identification on plant pentatricopeptide repeat proteins	118

Distant metastasis identification based on optimized graph representation of gene interaction patterns	117
Computational analyses of bacterial strains from shotgun reads	115
BayesKAT: bayesian optimal kernel-based test for genetic association studies reveals joint genetic effects in complex diseases	110
mbDecoda: a debiased approach to compositional data analysis for microbiome surveys	109
A robust statistical approach for finding informative spatially associated pathways	107
CpGFuse: a holistic approach for accurate identification of methylation states of DNA CpG sites	107
AptaDiff: de novo design and optimization of aptamers based on diffusion models	103
QOT: Quantized Optimal Transport for sample-level distance matrix in single-cell omics	102
Exploring the immune evasion of SARS-CoV-2 variant harboring E484K by molecular dynamics simulations	101
A chronotherapeutics-applicable multi-target therapeutics based on AI: Example of therapeutic hypothermia	100
Correction to: Addressing barriers in comprehensiveness, accessibility, reusability, interoperability and reproducibility of computational models in systems biology	97
PMiSLocMF: predicting miRNA subcellular localizations by incorporating multi-source features of miRNAs	96
Ensemble learning based on matrix completion improves microbe-disease association prediction	96
Inferring disease-associated circRNAs by multi-source aggregation based on heterogeneous graph neural network	94
Directed evolution of antimicrobial peptides using multi-objective zeroth-order optimization	94
Building multiscale models with PhysiBoSS, an agent-based modeling tool	93
Addressing scalability and managing sparsity and dropout events in single-cell representation identification with ZIGACL	93
Integrating AlphaFold and deep learning for atomistic interpretation of cryo-EM maps	90
A social theory-enhanced graph representation learning framework for multitask prediction of drug–drug interactions	89
dHICA: a deep transformer-based model enables accurate histone imputation from chromatin accessibility	89
Protein phosphorylation database and prediction tools	87
From intuition to AI: evolution of small molecule representations in drug discovery	86
scGAD: a new task and end-to-end framework for generalized cell type annotation and discovery	86
ADENet: a novel network-based inference method for prediction of drug adverse events	84
Large-scale predicting protein functions through heterogeneous feature fusion	84
Identification of vital chemical information via visualization of graph neural networks	84
MicroHDF: predicting host phenotypes with metagenomic data using a deep forest-based framework	82
Assessing protein model quality based on deep graph coupled networks using protein language model	82
HighFold: accurately predicting structures of cyclic peptides and complexes with head-to-tail and disulfide bridge constraints	81
Machine learning modeling of RNA structures: methods, challenges and future perspectives	81
Improving the performance of single-cell RNA-seq data mining based on relative expression orderings	80
Multiple errors correction for position-limited DNA sequences with GC balance and no homopolymer for DNA-based data storage	80
Clover: tree structure-based efficient DNA clustering for DNA-based data storage	78
Machine learning methods, databases and tools for drug combination prediction	78
Melanoma 2.0. Skin cancer as a paradigm for emerging diagnostic technologies, computational modelling and artificial intelligence	77
Subtype-DCC: decoupled contrastive clustering method for cancer subtype identification based on multi-omics data	77
Improving drug response prediction via integrating gene relationships with deep learning	77
Predicting MHC class I binder: existing approaches and a novel recurrent neural network solution	76
ULDNA: integrating unsupervised multi-source language models with LSTM-attention network for high-accuracy protein–DNA binding site prediction	75
Learning discriminative and structural samples for rare cell types with deep generative model	74
Circular RNAs and complex diseases: from experimental results to computational models	74
Deep learning in integrating spatial transcriptomics with other modalities	73
Benchmarking of computational methods for m6A profiling with Nanopore direct RNA sequencing	73
A robust and scalable graph neural network for accurate single-cell classification	73
Detecting tipping points of complex diseases by network information entropy	72
PRIEST: predicting viral mutations with immune escape capability of SARS-CoV-2 using temporal evolutionary information	72
A review on the application of bioinformatics tools in food microbiome studies	71
Evaluating large language models for annotating proteins	71