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Kingshuk Roy Choudhury

Publications and source records attributed to Kingshuk Roy Choudhury.

3 recordsLinked to original sources

Bayesian Modeling of the Structural Connectome for Studying Alzheimer Disease

We study possible relations between the structure of the connectome, white matter connecting different regions of brain, and Alzheimer disease. Regression models in covariates including age, gender and disease status for the extent of white matter connecting each pair of regions of brain are proposed. Subject We study possible relations between the Alzheimer's disease progression and the structure of the connectome, white matter connecting different regions of brain. Regression models in covariates including age, gender and disease status for the extent of white matter connecting each pair of regions of brain are proposed. Subject inhomogeneity is also incorporated in the model through random effects with an unknown distribution. As there are large number of pairs of regions, we also adopt a dimension reduction technique through graphon (Lovasz and Szegedy (2006)) functions, which reduces functions of pairs of regions to functions of regions. The connecting graphon functions are considered unknown but assumed smoothness allows putting priors of low complexity on them. We pursue a nonparametric Bayesian approach by assigning a Dirichlet process scale mixture of zero mean normal prior on the distributions of the random effects and finite random series of tensor products of B-splines priors on the underlying graphon functions. Markov chain Monte Carlo techniques, for drawing samples for the posterior distributions are developed. The proposed Bayesian method overwhelmingly outperforms similar ANCOVA models in the simulation setup. The proposed Bayesian approach is applied on a dataset of 100 subjects and 83 brain regions and key regions implicated in the changing connectome are identified.

stat.ME↗

High-dimensional single-index Bayesian modeling of brain atrophy

We propose a model of brain atrophy as a function of high-dimensional genetic information and low dimensional covariates such as gender, age, APOE gene, and disease status. A nonparametric single-index Bayesian model of high dimension is proposed to model the relationship with B-spline series prior on the unknown functions and Dirichlet process scale mixture of centered normal prior on the distributions of the random effects. The posterior rate of contraction without the random effect is established for a fixed number of regions and time points with increasing sample size. We implement an efficient computation algorithm through a Hamiltonian Monte Carlo (HMC) algorithm. The performance of the proposed Bayesian method is compared with the corresponding least square estimator in the linear model with horseshoe prior, LASSO and SCAD penalization on the high-dimensional covariates. The proposed Bayesian method is applied to a dataset on volumes of brain regions recorded over multiple visits of 748 individuals using 620,901 SNPs and 6 other covariates for each individual, to identify factors associated with brain atrophy.

stat.ME↗

Analysis of spatial distribution of marker expression in cells using boundary distance plots

Boundary distance (BD) plotting is a technique for making orientation invariant comparisons of the spatial distribution of biochemical markers within and across cells/nuclei. Marker expression is aggregated over points with the same distance from the boundary. We present a suite of tools for improved data analysis and statistical inference using BD plotting. BD is computed using the Euclidean distance transform after presmoothing and oversampling of nuclear boundaries. Marker distribution profiles are averaged using smoothing with linearly decreasing bandwidth. Average expression curves are scaled and registered by x-axis dilation to compensate for uneven lighting and errors in nuclear boundary marking. Penalized discriminant analysis is used to characterize the quality of separation between average marker distributions. An adaptive piecewise linear model is used to compare expression gradients in intra, peri and extra nuclear zones. The techniques are illustrated by the following: (a) a two sample problem involving a pair of voltage gated calcium channels (Cav1.2 and AB70) marked in different cells; (b) a paired sample problem of calcium channels (Y1F4 and RyR1) marked in the same cell.

stat.AP↗