Biodata Mining

Papers
(The TQCC of Biodata Mining is 4. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
Correction: Predictive modeling of ALS progression: an XGBoost approach using clinical features258
Transcriptome- and DNA methylation-based cell-type deconvolutions produce similar estimates of differential gene expression and differential methylation189
QIGTD: identifying critical genes in the evolution of lung adenocarcinoma with tensor decomposition46
A deep learning approach for classifying and predicting children's nutritional status in Ethiopia using LSTM-FC neural networks39
Processing imbalanced medical data at the data level with assisted-reproduction data as an example39
Saliency-driven explainable deep learning in medical imaging: bridging visual explainability and statistical quantitative analysis34
Neural network-based prognostic predictive tool for gastric cardiac cancer: the worldwide retrospective study28
Modeling heterogeneity of Sudanese hospital stay in neonatal and maternal unit: non-parametric random effect models with Gamma distribution23
An unsupervised image segmentation algorithm for coronary angiography22
Correction: Detection and classification of long terminal repeat sequences in plant LTR-retrotransposons and their analysis using explainable machine learning22
Machine learning and statistical approaches for classification of risk of coronary artery disease using plasma cytokines20
A new pipeline for structural characterization and classification of RNA-Seq microbiome data19
A maximum flow-based network approach for identification of stable noncoding biomarkers associated with the multigenic neurological condition, autism18
Taxonomy-based data representation for data mining: an example of the magnitude of risk associated with H. pylori infection14
LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genes13
Machine learning based study for the classification of Type 2 diabetes mellitus subtypes13
Disclosing transcriptomics network-based signatures of glioma heterogeneity using sparse methods10
Ensemble feature selection and tabular data augmentation with generative adversarial networks to enhance cutaneous melanoma identification and interpretability10
Exploring glioma heterogeneity through omics networks: from gene network discovery to causal insights and patient stratification9
Deep joint learning diagnosis of Alzheimer’s disease based on multimodal feature fusion9
Interaction models matter: an efficient, flexible computational framework for model-specific investigation of epistasis9
Transcriptome-based network analysis related to regulatory T cells infiltration identified RCN1 as a potential biomarker for prognosis in clear cell renal cell carcinoma9
Investigating potential drug targets for IgA nephropathy and membranous nephropathy through multi-queue plasma protein analysis: a Mendelian randomization study based on SMR and co-localization analys9
Reference-free phylogeny from sequencing data9
Development of glaucoma predictive model and risk factors assessment based on supervised models8
A new challenge for data analytics: transposons8
Deciphering the tissue-specific functional effect of Alzheimer risk SNPs with deep genome annotation8
Open challenges and opportunities in federated foundation models towards biomedical healthcare8
eQTpLot: a user-friendly R package for the visualization of colocalization between eQTL and GWAS signals7
Machine learning approaches for the genomic prediction of rheumatoid arthritis and systemic lupus erythematosus7
Prescription pattern analysis of Type 2 Diabetes Mellitus: a cross-sectional study in Isfahan, Iran6
Electronic medical records imputation by temporal Generative Adversarial Network6
Detection of iron deficiency anemia by medical images: a comparative study of machine learning algorithms6
Unsupervised clustering based coronary artery segmentation6
iU-Net: a hybrid structured network with a novel feature fusion approach for medical image segmentation6
MOCAT: multi-omics integration with auxiliary classifiers enhanced autoencoder6
Novel digital approaches to the assessment of problematic opioid use5
mSRFR: a machine learning model using microalgal signature features for ncRNA classification5
Personalized single-cell networks: a framework to predict the response of any gene to any drug for any patient5
iGlioSub: an integrative transcriptomic and epigenomic classifier for glioblastoma molecular subtypes5
Learning and visualizing chronic latent representations using electronic health records5
Polygenic risk modeling of tumor stage and survival in bladder cancer5
Inferring protein from transcript abundances using convolutional neural networks5
Evaluating risk detection methods to uncover ontogenic-mediated adverse drug effect mechanisms in children5
Machine learning approaches to identify systemic lupus erythematosus in anti-nuclear antibody-positive patients using genomic data and electronic health records5
Humans and machines in biomedical knowledge curation: hypertrophic cardiomyopathy molecular mechanisms’ representation5
6mA-StackingCV: an improved stacking ensemble model for predicting DNA N6-methyladenine site4
DIVIS: a semantic DIstance to improve the VISualisation of heterogeneous phenotypic datasets4
Unsupervised encoding selection through ensemble pruning for biomedical classification4
Priority-Elastic net for binary disease outcome prediction based on multi-omics data4
ParticleChromo3D: a Particle Swarm Optimization algorithm for chromosome 3D structure prediction from Hi-C data4
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