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Fusing Dual-Event Data Sets for Mycobacterium tuberculosis Machine Learning Models and Their Evaluation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Combining Computational Methods for Hit to Lead Optimization in Mycobacterium Tuberculosis Drug Discovery
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Bayesian Models Leveraging Bioactivity and Cytotoxicity Information for Drug Discovery
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Computational databases, pathway and cheminformatics tools for tuberculosis drug discovery
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Rising standards for tuberculosis drug development
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High-throughput screening for inhibitors of Mycobacterium tuberculosis H37Rv
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High throughput screening of a library based on kinase inhibitor scaffolds against Mycobacterium tuberculosis H37Rv
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Comprehensive analysis of methods used for the evaluation of compounds against Mycobacterium tuberculosis
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Drug design by machine learning: support vector machines for pharmaceutical data analysis
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A High-Throughput Screen To Identify Inhibitors of ATP Homeostasis in Non-replicating Mycobacterium tuberculosis
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Identification of Novel Inhibitors of M. tuberculosis Growth Using Whole Cell Based High-Throughput Screening
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Combinatorial Lead Optimization of [1,2]-Diamines Based on Ethambutol as Potential Antituberculosis Preclinical Candidates
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Improved Naïve Bayesian Modeling of Numerical Data for Absorption, Distribution, Metabolism and Excretion (ADME) Property Prediction
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In silico Prediction of Chemical Ames Mutagenicity
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Combination of Similarity Rankings Using Data Fusion
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Comparison of Confirmed Inactive and Randomly Selected Compounds as Negative Training Examples in Support Vector Machine-Based Virtual Screening
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Global Bayesian Models for the Prioritization of Antitubercular Agents
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A Predictive Ligand-Based Bayesian Model for Human Drug-Induced Liver Injury
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Molecular Determinants of Ligand Selectivity for the Human Multidrug and Toxin Extruder Proteins MATE1 and MATE2-K
inferredcites →https://doi.org/10.1126/science.1106753openalex-snapshot
A Diarylquinoline Drug Active on the ATP Synthase of Mycobacterium tuberculosis
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New Small-Molecule Synthetic Antimycobacterials
inferredcites →https://doi.org/10.1146/annurev.pharmtox.45.120403.100120openalex-snapshot
THE MAGIC BULLETS AND TUBERCULOSIS DRUG TARGETS
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Search of Chemical Scaffolds for Novel Antituberculosis Agents
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Development of CYP3A4 Inhibition Models: Comparisons of Machine-Learning Techniques and Molecular Descriptors
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Using Extended-Connectivity Fingerprints with Laplacian-Modified Bayesian Analysis in High-Throughput Screening Follow-Up
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Bioclipse: an open source workbench for chemo- and bioinformatics
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Computational models for in-vitro anti-tubercular activity of molecules based on high-throughput chemical biology screening datasets
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Predictive models for anti-tubercular molecules using machine learning on high-throughput biological screening datasets
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Predicting cytotoxicity from heterogeneous data sources with Bayesian learning
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Towards interoperable and reproducible QSAR analyses: Exchange of datasets
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TB Mobile: a mobile app for anti-tuberculosis molecules with known targets
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Enhanced ranking of PknB Inhibitors using data fusion methods
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Predicting P-Glycoprotein-Mediated Drug Transport Based On Support Vector Machine and Three-Dimensional Crystal Structure of P-glycoprotein
inferredcites →https://doi.org/10.1371/journal.pone.0063240openalex-snapshot
Enhancing Hit Identification in Mycobacterium tuberculosis Drug Discovery Using Validated Dual-Event Bayesian Models
inferredcites →https://doi.org/10.2174/156802612804910287openalex-snapshot
Open Source Drug Discovery with Bioclipse
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Molecule Property Analyses of Active Compounds for Mycobacterium tuberculosis
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Comparing and Validating Machine Learning Models for Mycobacterium tuberculosis Drug Discovery
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Intrabacterial Metabolism Obscures the Successful Prediction of an InhA Inhibitor of Mycobacterium tuberculosis
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