Prediction of compounds that are active against a desired biological target is a common step in drug discovery efforts. Virtual screening methods seek some active-enriched fraction of a library for ex
These are the code and datasets to reproduce all findings from the following paper: Playe, B., Stoven, V. Evaluation of deep and shallow learning methods in chemogenomics for the prediction of drugs s
Mithramycin A in known to bind DNA but its exact cellular mechanism of action is still unclear. We used Affymatrix GenFlex_Tag_16K_V2 microarrays to profile sensitivity of genetically barcoded S. cere