I am a mathematical biologist interested in developing mathematically sound approaches to the analysis of high-throughput DNA sequencing data. To do this, I utilize and develop techniques from the fields of probability, compressed sensing, and optimization. I am particularly interested in developing methods to analyze genomic and metagenomic data.
Use the quick links to the right to access information such as my CV, or the links at the top of the page to access a list of publications, my Github repository, etc.
Along with collaborators at UCLA, we were able to detect a small, but significant amount of microbes in blood This is surprising since it's typically assumed that the immune system typically removes any microbial presence from human blood. I used a reference-free microbial community algorithm, called EMDeBruijn, to help corroborate the patterns we saw which included an increase in microbial diversity in schizophrenia patients. EMDeBruijn is a metric based on the Wasserstein metric (aka the Earth Mover's Distance) and a de Bruijn graph induced by the k-mers in a metagenomic DNA sample.
My recent work with the CAMI project was
I'm pleased to announce that we've recently been funded by the NIH National Center for Advancing Translational Sciences (NCATS) along with Steve Ramsey (Oregon State).
This work improves upon the so called "min hash" technique (a "probabilistic data analysis" method) to develop a very fast and efficient way to estimate the similarity of two sets of objects (in terms of how much they overlap). The approach we present is orders of magnitude faster (and uses orders of magnitude less space) when two data sets under consideration are of very different size. The kinds of sets we consider are sets of sub-strings (called k-mers) of DNA sequences from communities of microorganisms.
A gene regulatory network is basically a representation of how genes interact with each other. In this work, we develop the only (to date) method to assess the accuracy of so called "motif discovery algorithms" that seek to find important sub-networks of a given gene regulatory network. We develop a provably correct mathematical approach (based on a variety of metrics that say how close two matrices are to each other) and use this to assess the performance of a variety of motif discovery algorithms.