I build statistical models for high-dimensional, dependent, and non-Gaussian data — with a focus on recovering interpretable structure (interactions, dependence, causal direction) from messy biomedical measurements.
Directed acyclic graphs, directed trees, and generalized Bayesian inference for learning how variables drive one another.
Latent factor and graphical models that make feature interactions estimable — and let them vary with covariates.
Semiparametric models for how a whole outcome distribution shifts with covariates, including discontinuities at thresholds.
Methods built for sparse, zero-inflated, compositional count data, and for integrating several omics tables at once.
Recovers directed tree structure among taxa while respecting two features that break standard methods: excess zeros and the compositional constraint of sequencing counts.
Models how an entire outcome density changes with covariates while allowing the density to jump at a threshold.
Lets factor loadings depend on covariates, so estimated interactions between microbial features can shift across host characteristics rather than being held fixed.
Estimates and tests for a jump in a density at a cutoff — the object of interest in regression-discontinuity style designs.
A sparse group factor model that estimates interactions within and across several count tables at once, such as paired microbiome and metabolite measurements.
A zero-inflated multivariate rounded log-normal model that separates true absence from undersampling when estimating feature interactions.
# denotes equal contribution.