Principled biophysical modeling is a necessary foundation for analyzing RNA sequencing data. In recent years, higher quality data for other data modalities at single-cell resolution have become available. I present joint biophysical models combining two of these modalities, chromatin accessibility measurements (ATAC-seq) and protein counts, individually with single-cell transcriptomic data, and give preliminary data results. I consider the extension of biophysically motivated models to the field of phylogenetics. I present competing mechanistic hypotheses for gene expression evolution and test them via parametrized single-cell cross-species data. I also consider a physics-inspired model for population-level evolution via maternal effects and interacting subpopulations.
Catherine Felce (Mon,) studied this question.