Multidimensional unfolding methods are widely used for visualizing item response data. Such methods project respondents and items simultaneously onto a low-dimensional Euclidian space, in which respondents and items are represented by ideal points, with person-person, item-item, and person-item similarities being captured by the Euclidian distances between the points. In this paper, we study the visualization of multidimensional unfolding from a statistical perspective. We cast multidimensional unfolding into an estimation problem, where the respondent and item ideal points are treated as parameters to be estimated. An estimator is then proposed for the simultaneous estimation of these parameters. Asymptotic theory is provided for the recovery of the ideal points, shedding lights on the validity of model-based visualization. An alternating projected gradient descent algorithm is proposed for the parameter estimation. We provide two illustrative examples, one on users' movie rating and the other on senate roll call voting.

MOTIVATION: Protein expression profiling for differences indicative of early cancer holds promise for improving diagnostics. Due to their high dimensionality, statistical analysis of proteomic data from mass spectrometers is challenging in many aspects such as dimension reduction, feature subset selection as well as construction of classification rules. Search of an optimal feature subset, commonly known as the feature subset selection (FSS) problem, is an important step towards disease classification/diagnostics with biomarkers. METHODS: We develop a parsimonious threshold-independent feature selection (PTIFS) method based on the concept of area under the curve (AUC) of the receiver operating characteristic (ROC). To reduce computational complexity to a manageable level, we use a sigmoid approximation to the empirical AUC as the criterion function. Starting from an anchor feature, the PTIFS method selects a feature subset through an iterative updating algorithm. Highly correlated features that have similar discriminating power are precluded from being selected simultaneously. The classification rule is then determined from the resulting feature subset. RESULTS: The performance of the proposed approach is investigated by extensive simulation studies, and by applying the method to two mass spectrometry data sets of prostate cancer and of liver cancer. We compare the new approach with the threshold gradient descent regularization (TGDR) method. The results show that our method can achieve comparable performance to that of the TGDR method in terms of disease classification, but with fewer features selected. AVAILABILITY: Supplementary Material and the PTIFS implementations are available at http://staff.ustc.edu.cn/~ynyang/PTIFS. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.