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.

This paper studies hypothesis testing and parameter estimation in the context of the divide-and-conquer algorithm. In a unified likelihood based framework, we propose new test statistics and point estimators obtained by aggregating various statistics from k subsamples of size n/k, where n is the sample size. In both low dimensional and sparse high dimensional settings, we address the important question of how large k can be, as n grows large, such that the loss of efficiency due to the divide-and-conquer algorithm is negligible. In other words, the resulting estimators have the same inferential efficiencies and estimation rates as an oracle with access to the full sample. Thorough numerical results are provided to back up the theory.

We examine the effect of errors in covariates in nonparametric function estimation. These functions include densities, regressions and conditional quantiles. To estimate these functions, we use the idea of deconvoluting kernels in conjunction with the ordinary kernel methods. We also discuss a new class of function estimators based on local polynomials.

Stem cell therapies have had tremendous potential application for many diseases in recent years. However, the tumorigeneic properties of stem cells restrict their potential clinical application; therefore, strategies for reducing the tumorigenic potential of stem cells must be established prior to transplantation. We have demonstrated that syngeneic transplantation of embryonic stem cells (ESCs) provokes an inflammatory response that involves the rapid recruitment of bone marrow-derived macrophages (BMDMs). ESCs are able to prevent mature macrophages from macrophage colony-stimulating factor (M-CSF) withdrawal-induced apoptosis, and thus prolong macrophage lifespan significantly by blocking various apoptotic pathways in an M-CSF-independent manner. ESCs express and secrete IL-34 which may be responsible for ESC-promoted macrophage survival. This anti-apoptotic effect of ESCs involves activation of extracellular signal-regulated kinase (ERK)1/2 and PI3K/Akt pathways and thus, inhibition of ERK1/2 and PI3K/AKT activation decreases ESC-induced macrophage survival. Functionally, ESC-treated macrophages also showed a higher level of phagocytic activity. ESCs further serve to polarize BMDMs into M2-like macrophages that exhibit most tumor-associated macrophage (TAM) phenotypic and functional features. ESC-educated macrophages produce high levels of arginase-1, Tie-2 and TNF-, which participate in angiogenesis and contribute to teratoma progression. Our study suggests that induction of M2-like macrophage activation is an important mechanism for teratoma development. Strategies targeting macrophages to

We derive the asymptotic distributions of the spiked eigenvalues and eigenvectors under a generalized and unified asymptotic regime, which takes into account the spike magnitude of leading eigenvalues, sample size, and dimensionality. This new regime allows high dimensionality and diverging eigenvalue spikes and provides new insights into the roles the leading eigenvalues, sample size, and dimensionality play in principal component analysis. The results are proven by a technical device, which swaps the role of rows and columns and converts the high-dimensional problems into low-dimensional ones. Our results are a natural extension of those in Paul (2007) to more general setting with new insights and solve the rates of convergence problems in Shen et al.(2013). They also reveal the biases of the estimation of leading eigenvalues and eigenvectors by using principal component analysis, and lead to a new covariance estimator for the approximate factor model, called shrinkage principal orthogonal complement thresholding (S-POET), that corrects the biases. Our results are successfully applied to outstanding problems in estimation of risks of large portfolios and false discovery proportions for dependent test statistics and are illustrated by simulation studies.