All Stories

  1. A Transformer-Based Model to Predict Micro RNA Interactions
  2. Modular Deep Neural Networks with Residual Connections for Predicting the Pathogenicity of Genetic Variants in Non Coding Genomic Regions
  3. AI methods and biologically informed data curation enable accurate RNA m5C prediction
  4. Replacing non-biomedical concepts improves embedding of biomedical concepts
  5. miss-SNF: a multimodal patient similarity network integration approach to handle completely missing data sources
  6. miss-SNF: a multimodal patient similarity network integration approach to handle completely missing data sources
  7. RNA Knowledge-Graph analysis through homogeneous embedding methods
  8. Fine-tuning of conditional Transformers improves in silico enzyme prediction and generation
  9. RNA knowledge-graph analysis through homogeneous embedding methods
  10. Leveraging generative AI to assist biocuration of medical actions for rare disease
  11. Fine-tuning of conditional Transformers for the generation of functionally characterized enzymes
  12. An ontology-based knowledge graph for representing interactions involving RNA molecules
  13. Systematic benchmarking demonstrates large language models have not reached the diagnostic accuracy of traditional rare-disease decision support tools
  14. Replacing non-biomedical concepts improves embedding of biomedical concepts
  15. Predicting nutrition and environmental factors associated with female reproductive disorders using a knowledge graph and random forests
  16. Association of post-COVID phenotypic manifestations with new-onset psychiatric disease
  17. An open source knowledge graph ecosystem for the life sciences
  18. Exploring the similarity between genetic diseases improves their differential diagnosis and the understanding of their etiology
  19. Intrinsic-Dimension analysis for guiding dimensionality reduction and data-fusion in multi-omics data processing
  20. Node-degree aware edge sampling mitigates inflated classification performance in biomedical random walk-based graph representation learning
  21. The promises of large language models for protein design and modeling
  22. Predictive models of long COVID
  23. Predicting nutrition and environmental factors associated with female reproductive disorders using a knowledge graph and random forests
  24. A software resource for large graph processing and analysis
  25. GRAPE for fast and scalable graph processing and random-walk-based embedding
  26. An expectation–maximization framework for comprehensive prediction of isoform-specific functions
  27. Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach
  28. A Meta-Graph for the Construction of an RNA-Centered Knowledge Graph
  29. Degree-Normalization Improves Random-Walk-Based Embedding Accuracy in PPI Graphs
  30. Integration and Visual Analysis of Biomolecular Networks Through UNIPred-Web
  31. Boosting tissue-specific prediction of active cis-regulatory regions through deep learning and Bayesian optimization techniques
  32. Metformin is Associated with Reduced COVID-19 Severity in Patients with Prediabetes
  33. GraPE: fast and scalable Graph Processing and Embedding
  34. Automated image analysis to assess hygienic behaviour of honeybees
  35. ParSMURF-NG: A Machine Learning High Performance Computing System for the Analysis of Imbalanced Big Omics Data
  36. Abdominal Computed Tomography Imaging Findings in Hospitalized COVID-19 Patients: A Year-Long Experience and Associations Revealed by Explainable Artificial Intelligence
  37. HEMDAG: a family of modular and scalable hierarchical ensemble methods to improve Gene Ontology term prediction
  38. NSAID use and clinical outcomes in COVID-19 patients: A 38-center retrospective cohort study
  39. Interpretable prioritization of splice variants in diagnostic next-generation sequencing
  40. Semi-automatic Column Type Inference for CSV Table Understanding
  41. Multi-resolution visualization and analysis of biomolecular networks through hierarchical community detection and web-based graphical tools
  42. Protein function prediction as a graph-transduction game
  43. Complex Data Imputation by Auto-Encoders and Convolutional Neural Networks—A Case Study on Genome Gap-Filling
  44. Multitask Hopfield Networks
  45. Disease–Genes Must Guide Data Source Integration in the Gene Prioritization Process
  46. Ensembling Descendant Term Classifiers to Improve Gene - Abnormal Phenotype Predictions
  47. Prediction of Human Phenotype Ontology terms by means of hierarchical ensemble methods
  48. Imbalance-Aware Machine Learning for Predicting Rare and Common Disease-Associated Non-Coding Variants
  49. COSNet: An R package for label prediction in unbalanced biological networks
  50. Within network learning on big graphs using secondary memory-based random walk kernels
  51. Multi-species protein function prediction
  52. An expanded evaluation of protein function prediction methods shows an improvement in accuracy
  53. A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
  54. RANKS: a flexible tool for node label ranking and classification in biological networks
  55. UNIPred: Unbalance-Aware Network Integration and Prediction of Protein Functions
  56. Learning node labels with multi-category Hopfield networks
  57. A Hierarchical Ensemble Method for DAG-Structured Taxonomies
  58. An extensive analysis of disease-gene associations using network integration and fast kernel-based gene prioritization methods
  59. Hierarchical Ensemble Methods for Protein Function Prediction
  60. Think globally and solve locally: secondary memory-based network learning for automated multi-species function prediction
  61. GOssTo: a stand-alone application and a web tool for calculating semantic similarities on the Gene Ontology
  62. Network-Based Drug Ranking and Repositioning with Respect to DrugBank Therapeutic Categories
  63. Energy‐Efficient Resource Utilization in Cloud Computing
  64. A neural network algorithm for semi-supervised node label learning from unbalanced data
  65. A Novel Approach to the Problem of Non-uniqueness of the Solution in Hierarchical Clustering
  66. Regeneration-associated WNT Signaling Is Activated in Long-term Reconstituting AC133bright Acute Myeloid Leukemia Cells
  67. A Fast Ranking Algorithm for Predicting Gene Functions in Biomolecular Networks
  68. Cancer module genes ranking using kernelized score functions
  69. Ensemble Methods
  70. Large Scale Ranking and Repositioning of Drugs with Respect to DrugBank Therapeutic Categories
  71. Random Walking on Functional Interaction Networks to Rank Genes Involved in Cancer
  72. Synergy of multi-label hierarchical ensembles, data fusion, and cost-sensitive methods for gene functional inference
  73. A Mathematical Model for the Validation of Gene Selection Methods
  74. True Path Rule Hierarchical Ensembles for Genome-Wide Gene Function Prediction
  75. XML-Based Approaches for the Integration of Heterogeneous Bio-Molecular Data
  76. Ensembles in Machine Learning Applications
  77. COSNet: A Cost Sensitive Neural Network for Semi-supervised Learning in Graphs
  78. A Novel Ensemble Technique for Protein Subcellular Location Prediction
  79. Learning functional linkage networks with a cost-sensitive approach
  80. Dynamic multi-objective routing algorithm: a multi-objective routing algorithm for the simple hybrid routing protocol on wireless sensor networks
  81. Integration of heterogeneous data sources for gene function prediction using decision templates and ensembles of learning machines
  82. An Experimental Comparison of Hierarchical Bayes and True Path Rule Ensembles for Protein Function Prediction
  83. XML-based approaches for the integration of heterogeneous bio-molecular data
  84. Classification of co-expressed genes from DNA regulatory regions
  85. Computational intelligence and machine learning in bioinformatics
  86. Fuzzy ensemble clustering based on random projections for DNA microarray data analysis
  87. Applications of Supervised and Unsupervised Ensemble Methods
  88. True Path Rule Hierarchical Ensembles
  89. Ensemble Based Data Fusion for Gene Function Prediction
  90. A stability-based algorithm to validate hierarchical clusters of genes
  91. Unsupervised Stability-Based Ensembles to Discover Reliable Structures in Complex Bio-molecular Data
  92. Prediction of Gene Function Using Ensembles of SVMs and Heterogeneous Data Sources
  93. Classification of DNA microarray data with Random Projection Ensembles of Polynomial SVMs
  94. Comparing early and late data fusion methods for gene function prediction
  95. Dataset complexity can help to generate accurate ensembles of k-nearest neighbors
  96. Discovering multi–level structures in bio-molecular data through the Bernstein inequality
  97. HCGene: a software tool to support the hierarchical classification of genes
  98. Supervised and Unsupervised Ensemble Methods and their Applications
  99. Ensemble Clustering with a Fuzzy Approach
  100. Gene expression modeling through positive boolean functions
  101. Model order selection for bio-molecular data clustering
  102. Discovering Significant Structures in Clustered Bio-molecular Data Through the Bernstein Inequality
  103. Mosclust: a software library for discovering significant structures in bio-molecular data
  104. Randomized maps for assessing the reliability of patients clusters in DNA microarray data analyses
  105. Characterization of lung tumor subtypes through gene expression cluster validity assessment
  106. Ensembles Based on Random Projections to Improve the Accuracy of Clustering Algorithms
  107. Biological Specifications for a Synthetic Gene Expression Data Generation Model
  108. Clusterv: a tool for assessing the reliability of clusters discovered in DNA microarray data
  109. An Experimental Bias-Variance Analysis of SVM Ensembles Based on Resampling Techniques
  110. Support vector machines for candidate nodules classification
  111. Bio-molecular cancer prediction with random subspace ensembles of support vector machines
  112. Lung nodules detection and classification
  113. An experimental analysis of the dependence among codeword bit errors in ECOC learning machines
  114. Effectiveness of error correcting output coding methods in ensemble and monolithic learning machines
  115. Cancer recognition with bagged ensembles of support vector machines
  116. Random Aggregated and Bagged Ensembles of SVMs: An Empirical Bias–Variance Analysis
  117. Effectiveness of error correcting output coding methods in ensemble and monolithic learning machines
  118. An Application of Low Bias Bagged SVMs to the Classification of Heterogeneous Malignant Tissues
  119. Gene expression data analysis of human lymphoma using support vector machines and output coding ensembles
  120. NEURObjects: an object-oriented library for neural network development
  121. Ensembles of Learning Machines
  122. Boosting and Classification of Electronic Nose Data
  123. Bias—Variance Analysis and Ensembles of SVM
  124. Decompositive classification models for electronic noses
  125. Dependence among Codeword Bits Errors in ECOC Learning Machines: An Experimental Analysis
  126. Effectiveness of Error Correcting Output Codes in Multiclass Learning Problems
  127. Feature Selection Combined with Random Subspace Ensemble for Gene Expression Based Diagnosis of Malignancies
  128. Fuzzy Ensemble Clustering for DNA Microarray Data Analysis
  129. An Algorithm to Assess the Reliability of Hierarchical Clusters in Gene Expression Data
  130. Data Integration Issues and Opportunities in Biological XML Data Management
  131. Bagged ensembles of Support Vector Machines for gene expression data analysis
  132. Random projections for assessing gene expression cluster stability