Jonah R. Huggins

The paper develops an algorithm to simulate and compare mechanistic models of cell viability assays with experimental data to understand drug response variability.

This paper introduces genetically-encoded fluorescence barcodes using spectral flow cytometry for single-cell analysis, demonstrating high classification accuracy for most barcodes.

This paper introduces a 96-sample western blot format that improves efficiency and capacity while maintaining compatibility with standard protocols.

The paper uses multiomic data to identify cell state transitions in GBM and proposes potential drug targets to alter these transitions.

The paper improves fluorescent antibody labeling to enhance signal intensity for multiplex flow cytometry, showing internal labeling increases brightness and enables triple staining.

The paper develops two solutions to communication bottlenecks in large-scale single-cell models, significantly speeding up simulations.