Discrepancy is a kind of important measure used in experimental design. Recently, a so-called discrete discrepancy has been applied to evaluate the uniformity of factorial designs. In this paper, we review some recent advances on application of the discrete discrepancy to several common experimental designs and summarize some important results.

Cryo-electron microscopy (cryo-EM) has recently emerged as a powerful tool for obtaining three-dimensional (3D) structures of biological macromolecules in native states. A minimum cryo-EM image data set for deriving a meaningful reconstruction is comprised of thousands of randomly orientated projections of identical particles photographed with a small number of electrons. The computation of 3D structure from 2D projections requires clustering, which aims to enhance the signal to noise ratio in each view by grouping similarly oriented images. Nevertheless, the prevailing clustering techniques are often compromised by three characteristics of cryo-EM data: high noise content, high dimensionality and large number of clusters. Moreover, since clustering requires registering images of similar orientation into the same pixel coordinates by 2D alignment, it is desired that the clustering algorithm can label misaligned images as outliers. Herein, we introduce a clustering algorithm γ-SUP to model the data with a q-Gaussian mixture and adopt the minimum γ-divergence for estimation, and then use a self-updating procedure to obtain the numerical solution. We apply γ-SUP to the cryo-EM images of two benchmark macromolecules, RNA polymerase II and ribosome. In the former case, simulated images were chosen to decouple clustering from alignment to demonstrate γ-SUP is more robust to misalignment outliers than the existing clustering methods used in the cryo-EM community. In the latter case, the clustering of real cryo-EM data by our γ-SUP method eliminates noise in many views to reveal true structure features of ribosome at the projection level.

In this chapter, we give a selective review of the nonparametric modeling methods using Cox's type of models in survival analysis. We first introduce Cox's model (Cox 1972) and then study its variants in the direction of smoothing. The model fitting, variable selection, and hypothesis testing problems are addressed. A number of topics worthy of further study are given throughout this chapter.

In this note we include a correction for Equation (19) on page 840 which is a step in the proof of Theorem 4 of Fan et al.(2014). There is no change in the statement of Theorem 4, and the rest of the proof stays unchanged. Equation (19) on page 840 should be corrected to as follows: We apply the coordinatewise mean-value theorem with respect to each coordinate of (ie, j) to obtain that

This paper is concerned with the problem of top- K ranking from pairwise comparisons. Given a collection of K items and a few pairwise comparisons across them, one wishes to identify the set of K items that receive the highest ranks. To tackle this problem, we adopt the logistic parametric model---the Bradley-Terry-Luce model, where each item is assigned a latent preference score, and where the outcome of each pairwise comparison depends solely on the relative scores of the two items involved. Recent works have made significant progress towards characterizing the performance (eg the mean square error for estimating the scores) of several classical methods, including the spectral method and the maximum likelihood estimator (MLE). However, where they stand regarding top- K ranking remains unsettled.