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Raymond Carroll

Publications and source records attributed to Raymond Carroll.

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Surrogate Aided Unsupervised Recovery of Sparse Signals in Single Index Models for Binary Outcomes

We consider the recovery of regression coefficients, denoted by $\boldsymbol{\beta}_0$, for a single index model (SIM) relating a binary outcome $Y$ to a set of possibly high dimensional covariates $\boldsymbol{X}$, based on a large but 'unlabeled' dataset $\mathcal{U}$, with $Y$ never observed. On $\mathcal{U}$, we fully observe $\boldsymbol{X}$ and additionally, a surrogate $S$ which, while not being strongly predictive of $Y$ throughout the entirety of its support, can forecast it with high accuracy when it assumes extreme values. Such datasets arise naturally in modern studies involving large databases such as electronic medical records (EMR) where $Y$, unlike $(\boldsymbol{X}, S)$, is difficult and/or expensive to obtain. In EMR studies, an example of $Y$ and $S$ would be the true disease phenotype and the count of the associated diagnostic codes respectively. Assuming another SIM for $S$ given $\boldsymbol{X}$, we show that under sparsity assumptions, we can recover $\boldsymbol{\beta}_0$ proportionally by simply fitting a least squares LASSO estimator to the subset of the observed data on $(\boldsymbol{X}, S)$ restricted to the extreme sets of $S$, with $Y$ imputed using the surrogacy of $S$. We obtain sharp finite sample performance bounds for our estimator, including deterministic deviation bounds and probabilistic guarantees. We demonstrate the effectiveness of our approach through multiple simulation studies, as well as by application to real data from an EMR study conducted at the Partners HealthCare Systems.

stat.ME

Feature selection for high-dimensional integrated data

Motivated by the problem of identifying correlations between genes or features of two related biological systems, we propose a model of \emph{feature selection} in which only a subset of the predictors $X_t$ are dependent on the multidimensional variate $Y$, and the remainder of the predictors constitute a "noise set" $X_u$ independent of $Y$. Using Monte Carlo simulations, we investigated the relative performance of two methods: thresholding and singular-value decomposition, in combination with stochastic optimization to determine "empirical bounds" on the small-sample accuracy of an asymptotic approximation. We demonstrate utility of the thresholding and SVD feature selection methods to with respect to a recent infant intestinal gene expression and metagenomics dataset.

stat.AP