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6 April 2009:
I successfully defended my thesis!

Systems biology:

- Lingchong You
- Duke ICBP

Syndromic surveillance:

- ISDS

Statistical areas:

Primarily I am interested in models, methods, and computation in Bayesian analysis broadly with current focuses in time series analysis and dynamic models. Specifically this includes filtering and smoothing in state-space models using either Markov chain Monte Carlo for batch analysis or sequential Monte Carlo methods for real-time analysis.

Filtering

sequential particle filtering 95% credible intervals and median
for a fixed parameter Filtering occurs in dynamic models, often referred to as state-space models, where the objective is to determine the distribution of the latent state and fixed parameters given all the data up to that time. I create methodology for both analytical and simulated approximations to this distribution for non-linear and non-Gaussian models. The picture plots the 95% credible interval and median for three different approximations to the filtered distribution for a fixed parameter.

Smoothing

bivariate smoothing distribution for two consecutive states Smoothing occurs in dynamic models where the objective is to determine the distribution of the latent state and fixed parameters given all the data (not just data up to a particular time). I create approximations to this distribution for non-linear and non-Guassian models. The picture plots the bivariate distribution between two consecutive states. The high degree of multimodality depicted shows the non-trivial nature of these problems.


Applied areas:

Dynamic models have wide application and here I describe a few applied areas of my research.

Systems biology

Systems biology studies the dynamics of cellular function. I build models to represent the fluctuations of protein levels within cells. These models are non-linear, multivariate processes that include both intrinsic and extrinsic noise as well as measurement error. The picture shows a snapshot of bacterial cells using fluorescence microscopy, green brightness indicates the level of a particular protein.

Syndromic surveillance

In syndromic surveillance the goal is to have an alert system that quickly detects an outbreak of both known and unknown diseases. I build models representing the baseline fluctuation as well as outbreak profiles for a variety of diseases. The picture to the right shows a reporting system with the observations as points, outbreak period shown in red, and the blue line indicating the alert system.

Drug abuse trends

The goal of this research was to build a system based on national databases that could detect a change in opioid drug abuse rates. There is known spatial hetergeneity that we accounted for using random effects for states in a conditionally autoregressive model. The picture shows a map of the posterior median for these random effects where red indicates high abuse and blue indicates low abuse.