0000000000586227

AUTHOR

Martin Gütlein

showing 9 related works from this author

Optimization of curation of the dataset with data on repeated dose toxicity

2015

Introduction: For some areas of risk assessment, the use of alter-native methods is supported by current directives and guidance(e.g. REACH, Cosmetics, BPD, PPP). According to OECD principles alternative methods need to be scientifically valid. Methods: Within a project on grouping and development of predictive models sup-ported by a grant of Federal Ministry of Education and Research, we curated a dataset based on RepDose and ELINCS database. The final dataset consists of rat repeated dose toxicity studies for 1022 com-pounds representing 28 endpoints as organ-effect-combinations. Toxicological and modelling experts did jointly the curation and selection of endpoints as an iterative proces…

business.industryToxicityMedicineGeneral MedicineToxicologyBioinformaticsbusinessToxicology Letters
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Innovative Strategies to Develop Chemical Categories Using a Combination of Structural and Toxicological Properties.

2016

Interest is increasing in the development of non-animal methods for toxicological evaluations. These methods are however, particularly challenging for complex toxicological endpoints such as repeated dose toxicity. European Legislation, e.g., the European Union's Cosmetic Directive and REACH, demands the use of alternative methods. Frameworks, such as the Read-across Assessment Framework or the Adverse Outcome Pathway Knowledge Base, support the development of these methods. The aim of the project presented in this publication was to develop substance categories for a read-across with complex endpoints of toxicity based on existing databases. The basic conceptual approach was to combine str…

0301 basic medicineQuantitative structure–activity relationshipread acrossPredictive Clustering Tree (PCT) methodComputer science610010501 environmental sciencescomputer.software_genre600 Technik Medizin angewandte Wissenschaften::610 Medizin und Gesundheit01 natural sciences03 medical and health sciencesPharmacology (medical)Cluster analysis0105 earth and related environmental sciencesOriginal ResearchAlternative methodsPharmacologytoxicological and structural similaritybusiness.industryQSARlcsh:RM1-950non-animal methods; QSAR; readacross; Predictive Clustering Tree (PCT) method; toxicological and structural similarityIdentification (information)Tree (data structure)030104 developmental biologyConceptual approachlcsh:Therapeutics. PharmacologyKnowledge basenon-animal methodsData miningWeb servicebusinesscomputerFrontiers in pharmacology
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A Large-Scale Empirical Evaluation of Cross-Validation and External Test Set Validation in (Q)SAR.

2013

(Q)SAR model validation is essential to ensure the quality of inferred models and to indicate future model predictivity on unseen compounds. Proper validation is also one of the requirements of regulatory authorities in order to accept the (Q)SAR model, and to approve its use in real world scenarios as alternative testing method. However, at the same time, the question of how to validate a (Q)SAR model, in particular whether to employ variants of cross-validation or external test set validation, is still under discussion. In this paper, we empirically compare a k-fold cross-validation with external test set validation. To this end we introduce a workflow allowing to realistically simulate t…

Computer sciencemedia_common.quotation_subjectOrganic ChemistryScale (descriptive set theory)Variance (accounting)computer.software_genreCross-validationComputer Science ApplicationsModel validationWorkflowStructural BiologyCheminformaticsTest setDrug DiscoveryMolecular MedicineQuality (business)Data miningcomputermedia_commonMolecular informatics
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Eawag-Soil in enviPath: a new resource for exploring regulatory pesticide soil biodegradation pathways and half-life data.

2017

Developing models for the prediction of microbial biotransformation pathways and half-lives of trace organic contaminants in different environments requires as training data easily accessible and sufficiently large collections of respective biotransformation data that are annotated with metadata on study conditions. Here, we present the Eawag-Soil package, a public database that has been developed to contain all freely accessible regulatory data on pesticide degradation in laboratory soil simulation studies for pesticides registered in the EU (282 degradation pathways, 1535 reactions, 1619 compounds and 4716 biotransformation half-life values with corresponding metadata on study conditions)…

0301 basic medicine10120 Department of ChemistryDatabases FactualSoil biodegradation010501 environmental sciencesManagement Monitoring Policy and Law01 natural sciencesModels Biological03 medical and health sciencesSoilResource (project management)Biotransformation2308 Management Monitoring Policy and LawSoil retrogression and degradation540 ChemistryEnvironmental ChemistrySoil PollutantsPesticidesBiotransformation0105 earth and related environmental sciencesTraining setChemistryPublic Health Environmental and Occupational HealthGeneral Medicine2739 Public Health Environmental and Occupational Health15. Life on landPesticideMetadata030104 developmental biologyBiodegradation Environmental13. Climate actionEnvironmental chemistry2304 Environmental ChemistryPesticide degradationBiochemical engineeringHalf-LifeEnvironmental science. Processesimpacts
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enviPath - The environmental contaminant biotransformation pathway resource

2016

The University of Minnesota Biocatalysis/Biodegradation Database and Pathway Prediction System (UM-BBD/PPS) has been a unique resource covering microbial biotransformation pathways of primarily xenobiotic chemicals for over 15 years. This paper introduces the successor system, enviPath (The Environmental Contaminant Biotransformation Pathway Resource), which is a complete redesign and reimplementation of UM-BBD/PPS. enviPath uses the database from the UM-BBD/PPS as a basis, extends the use of this database, and allows users to include their own data to support multiple use cases. Relative reasoning is supported for the refinement of predictions and to allow its extensions in terms of previo…

User-Computer InterfaceBiocatalysisDatabase IssueEnvironmental PollutantsBiotransformationDatabases ChemicalXenobiotics
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Modeling Chronic Toxicity: A Comparison of Experimental Variability With (Q)SAR/Read-Across Predictions

2018

This study compares the accuracy of (Q)SAR/read-across predictions with the experimental variability of chronic lowest-observed-adverse-effect levels (LOAELs) from in vivo experiments. We could demonstrate that predictions of the lazy structure-activity relationships (lazar) algorithm within the applicability domain of the training data have the same variability as the experimental training data. Predictions with a lower similarity threshold (i.e., a larger distance from the applicability domain) are also significantly better than random guessing, but the errors to be expected are higher and a manual inspection of prediction results is highly recommended.

0301 basic medicinePharmacologyTraining setlazarbusiness.industrylcsh:RM1-950Pattern recognition010501 environmental sciences01 natural sciencesexperimental variability(Q)SAR03 medical and health sciences030104 developmental biologylcsh:Therapeutics. PharmacologySimilarity (network science)Pharmacology (medical)Artificial intelligencebusinessChronic toxicityLOAEL0105 earth and related environmental sciencesApplicability domainMathematicsread-acrossFrontiers in Pharmacology
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CheS-Mapper - Chemical Space Mapping and Visualization in 3D

2012

Abstract Analyzing chemical datasets is a challenging task for scientific researchers in the field of chemoinformatics. It is important, yet difficult to understand the relationship between the structure of chemical compounds, their physico-chemical properties, and biological or toxic effects. To that respect, visualization tools can help to better comprehend the underlying correlations. Our recently developed 3D molecular viewer CheS-Mapper (Chemical Space Mapper) divides large datasets into clusters of similar compounds and consequently arranges them in 3D space, such that their spatial proximity reflects their similarity. The user can indirectly determine similarity, by selecting which f…

Process (engineering)Computer sciencemedia_common.quotation_subjectLibrary and Information Sciencescomputer.software_genre01 natural scienceslcsh:Chemistry03 medical and health sciencesSimilarity (psychology)Physical and Theoretical ChemistryFunction (engineering)030304 developmental biologymedia_commonStructure (mathematical logic)0303 health scienceslcsh:T58.5-58.64lcsh:Information technology004 InformatikComputer Graphics and Computer-Aided DesignChemical spaceField (geography)0104 chemical sciencesVisualizationComputer Science Applications010404 medicinal & biomolecular chemistrylcsh:QD1-999CheminformaticsData miningcomputer004 Data processingSoftwareJournal of Cheminformatics
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CheS-Mapper 2.0 for visual validation of (Q)SAR models

2014

Abstract Background Sound statistical validation is important to evaluate and compare the overall performance of (Q)SAR models. However, classical validation does not support the user in better understanding the properties of the model or the underlying data. Even though, a number of visualization tools for analyzing (Q)SAR information in small molecule datasets exist, integrated visualization methods that allow the investigation of model validation results are still lacking. Results We propose visual validation, as an approach for the graphical inspection of (Q)SAR model validation results. The approach applies the 3D viewer CheS-Mapper, an open-source application for the exploration of sm…

Visualization methodsComputer scienceFeature vectorLibrary and Information Sciencescomputer.software_genre01 natural sciences(Q)SARModel validation03 medical and health sciencesSoftwareValidationOverall performancePhysical and Theoretical ChemistryVisualization030304 developmental biology0303 health sciencesbusiness.industryStatistical validationComputer Graphics and Computer-Aided Design0104 chemical sciencesComputer Science ApplicationsVisualization010404 medicinal & biomolecular chemistry3d space3D spaceData miningbusinesscomputerSoftwareJournal of Cheminformatics
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Filtered circular fingerprints improve either prediction or runtime performance while retaining interpretability

2016

Physical and Theoretical ChemistryLibrary and Information Sciences004 InformatikComputer Graphics and Computer-Aided Design004 Data processingComputer Science ApplicationsJournal of Cheminformatics
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