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“Bayes Affinity Fingerprints” Improve Retrieval Rates in Virtual Screening and Define Orthogonal Bioactivity Space: When Are Multitarget Drugs a Feasible Concept?
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Outgoing claims: the papers this work cites, builds on, or argues with.
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A Discussion of Measures of Enrichment in Virtual Screening: Comparing the Information Content of Descriptors with Increasing Levels of Sophistication
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“Bayes Affinity Fingerprints” Improve Retrieval Rates in Virtual Screening and Define Orthogonal Bioactivity Space: When Are Multitarget Drugs a Feasible Concept?
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Additional file 1 of QSAR-derived affinity fingerprints (part 2): modeling performance for potency prediction
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Additional file 1 of Merging bioactivity predictions from cell morphology and chemical fingerprint models using similarity to training data
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Additional file 2 of Merging bioactivity predictions from cell morphology and chemical fingerprint models using similarity to training data
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Additional file 3 of Merging bioactivity predictions from cell morphology and chemical fingerprint models using similarity to training data
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Additional file 4 of Merging bioactivity predictions from cell morphology and chemical fingerprint models using similarity to training data
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Additional file 5 of Merging bioactivity predictions from cell morphology and chemical fingerprint models using similarity to training data
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