Supervised learning of protein variant effects across large-scale mutagenesis datasets.

The increasing availability of data from multiplexed assays of variant effects (MAVEs) enables supervised model training against large quantities of experimental data to learn sequence-function relationships. Variant effect scores from MAVEs can, however, be influenced by the experimental method and library composition, resulting in experiment-to-experiment differences in the mapping from molecular level variant effects to MAVE readout. This variation presents a challenge for supervised learning across datasets that limits our ability to leverage the data generated by MAVEs. We here develop a framework for performing supervised learning with MAVE data that takes the influence of the experimental protocol into account, thus enabling variant effects to be learned across datasets produced in independent experiments. We apply the framework to train a model against variant effect scores collected with VAMP-seq, a MAVE technique that quantifies the steady-state cellular abundance of protein variants. Our results suggest that mapping variant abundance to VAMP-seq readout in a dataset-specific manner during model training improves the learned abundance model and moreover allows the learned model to predict variant effects on an interpretable scale. Our work highlights the importance of combining MAVE results with low-throughput experiments to facilitate MAVE score interpretation and supervised model training.