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Kieran R Campbell

Publications and source records attributed to Kieran R Campbell.

2 recordsLinked to original sources

Restricted Search Space Graph MCMC via Birth-Death Processes

Inferring directed acyclic graphs (DAGs) from data via Markov chain Monte Carlo (MCMC) is computationally challenging in moderate-to-high dimensional settings because their discrete sampling space grows super-exponentially with the number of nodes. To address scalability, several recent MCMC-based graph inference methods restrict the search space to a subset of edges, at the cost of introducing error into the inference procedure. In this work, we derive sharp lower and upper bounds on the total variation distance between the unrestricted posterior distribution and the posterior distribution induced by a state-of-the-art restricted search space MCMC method. These bounds characterize regimes in which the approximation error is negligible and regimes in which it is not. In order to reduce the error, we propose a flexible transdimensional MCMC sampler which allows the search space to expand or contract dynamically as the chain progresses. The sampler is defined by birth-and-death rates that induce a prior distribution on the set of search spaces, rather than assume a fixed restricted search space throughout. We outline an efficient implementation of the proposed algorithm and demonstrate its finite-sample performance through simulation studies.

stat.ME↗

Computational modelling in single-cell cancer genomics: methods and future directions

Single-cell technologies have revolutionized biomedical research by enabling scalable measurement of the genome, transcriptome, and proteome of multiple systems at single-cell resolution. Now widely applied to cancer models, these assays offer new insights into tumour heterogeneity, which underlies cancer initiation, progression, and relapse. However, the large quantities of high-dimensional, noisy data produced by single-cell assays can complicate data analysis, obscuring biological signals with technical artefacts. In this review article, we outline the major challenges in analyzing single-cell cancer genomics data and survey the current computational tools available to tackle these. We further outline unsolved problems that we consider major opportunities for future methods development to help interpret the vast quantities of data being generated.

q-bio.GN↗