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Bonnie Kirkpatrick

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2 papers
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2

ICML Conference 2014 Conference Paper

Efficient Continuous-Time Markov Chain Estimation

  • Monir Hajiaghayi
  • Bonnie Kirkpatrick
  • Liangliang Wang
  • Alexandre Bouchard-Côté

Many problems of practical interest rely on Continuous-time Markov chains (CTMCs) defined over combinatorial state spaces, rendering the computation of transition probabilities, and hence probabilistic inference, difficult or impossible with existing methods. For problems with countably infinite states, where classical methods such as matrix exponentiation are not applicable, the main alternative has been particle Markov chain Monte Carlo methods imputing both the holding times and sequences of visited states. We propose a particle-based Monte Carlo approach where the holding times are marginalized analytically. We demonstrate that in a range of realistic inferential setups, our scheme dramatically reduces the variance of the Monte Carlo approximation and yields more accurate parameter posterior approximations given a fixed computational budget. These experiments are performed on both synthetic and real datasets, drawing from two important examples of CTMCs having combinatorial state spaces: string-valued mutation models in phylogenetics and nucleic acid folding pathways.

NeurIPS Conference 2012 Conference Paper

Bayesian Pedigree Analysis using Measure Factorization

  • Bonnie Kirkpatrick
  • Alexandre Bouchard-Côté

Pedigrees, or family trees, are directed graphs used to identify sites of the genome that are correlated with the presence or absence of a disease. With the advent of genotyping and sequencing technologies, there has been an explosion in the amount of data available, both in the number of individuals and in the number of sites. Some pedigrees number in the thousands of individuals. Meanwhile, analysis methods have remained limited to pedigrees of <100 individuals which limits analyses to many small independent pedigrees. Disease models, such those used for the linkage analysis log-odds (LOD) estimator, have similarly been limited. This is because linkage anlysis was originally designed with a different task in mind, that of ordering the sites in the genome, before there were technologies that could reveal the order. LODs are difficult to interpret and nontrivial to extend to consider interactions among sites. These developments and difficulties call for the creation of modern methods of pedigree analysis. Drawing from recent advances in graphical model inference and transducer theory, we introduce a simple yet powerful formalism for expressing genetic disease models. We show that these disease models can be turned into accurate and efficient estimators. The technique we use for constructing the variational approximation has potential applications to inference in other large-scale graphical models. This method allows inference on larger pedigrees than previously analyzed in the literature, which improves disease site prediction.

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