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Similarity maps - a visualization strategy for molecular fingerprints and machine-learning methods.

, and . J. Cheminformatics, (2013)

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Bringing the MMFF force field to the RDKit: implementation and validation., , and . J. Cheminformatics, 6 (1): 37 (2014)Heterogeneous Classifier Fusion for Ligand-Based Virtual Screening: Or, How Decision Making by Committee Can Be a Good Thing., , and . Journal of Chemical Information and Modeling, 53 (11): 2829-2836 (2013)Development of a Novel Fingerprint for Chemical Reactions and Its Application to Large-Scale Reaction Classification and Similarity., , , and . Journal of Chemical Information and Modeling, 55 (1): 39-53 (2015)Corrections to "Development of a Novel Fingerprint for Chemical Reactions and Its Application to Large-Scale Reaction Classification and Similarity"., , , and . Journal of Chemical Information and Modeling, 55 (2): 474 (2015)Get your chemistry right with KNIME., and . J. Cheminformatics, 5 (S-1): 1 (2013)The integration of Open3DTOOLS into the RDKit and KNIME., , and . J. Cheminformatics, 6 (S-1): 8 (2014)Making sure there's a "give" associated with the "take": producing and using open-source software in big pharma., , , , and . J. Cheminformatics, 3 (S-1): 3 (2011)Feature-map vectors: a new class of informative descriptors for computational drug discovery., , and . Journal of Computer-Aided Molecular Design, 20 (12): 751-762 (2006)Get Your Atoms in Order - An Open-Source Implementation of a Novel and Robust Molecular Canonicalization Algorithm., , and . Journal of Chemical Information and Modeling, 55 (10): 2111-2120 (2015)What's What: The (Nearly) Definitive Guide to Reaction Role Assignment., , and . Journal of Chemical Information and Modeling, 56 (12): 2336-2346 (2016)