Frequentists' inference often delivers point estimators associated with condence intervals or sets for parameters of interest. Constructing the condence intervals or sets requires understanding the sampling distributions of the point estimators, which, in many but not all cases, are related to asymptotic Normal distributions ensured by central limit theorems. Although previous literature has established various forms of central limit theorems for statistical inference in super population models, we still need general and convenient forms of central limit theorems for some randomization-based causal analysis of experimental data, where the parameters of interests are functions of a nite population and randomness comes solely from the treatment assignment. We use central limit theorems for sample surveys and rank statistics to establish general forms of the nite population central limit theorems that are particularly useful for proving asymptotic distributions of randomization tests under the sharp null hypothesis of zero individual causal eects, and for obtaining the asymptotic repeated sampling distributions of the causal eect estimators. The new central limit theorems hold for general experimental designs with multiple treatment levels, multiple treatment factors and vector outcomes, and are immediately applicable for studying the asymptotic properties of many methods in causal inference, including instrumental variable, regression adjustment, rerandomization, clustered randomized experiments, and so on. Previously, the asymptotic properties of these problems are often based on heuristic arguments, which in fact rely on general forms of nite population central limit theorems that have not been established before. Our new theorems ll in this gap by providing more solid theoretical foundation for asymptotic randomization-based causal inference.

Due to vast sequence divergence among different viral groups, sequence alignment is not directly applicable to genome-wide comparative analysis of viruses. More and more attention has been paid to alignment-free methods for whole genome comparison and phylogenetic tree reconstruction. Among alignment-free methods, the recently proposed ‘‘Natural Vector (NV) representation” has successfully been used to study the phylogeny of multi-segmented viruses based on a 12-dimensional genome space derived from the nucleotide sequence structure. But the preference of proteomes over genomes for the determination of viral phylogeny was not deeply investigated. As the translated products of genes, proteins directly form the shape of viral structure and are vital for all metabolic pathways. In this study, using the NV representation of a protein sequence along with the Hausdorff distance suitable to compare point sets, we construct a 60-dimensional protein space to analyze the evolutionary relationships of 4021 viruses by whole-proteomes in the current NCBI Reference Sequence Database (RefSeq). We also take advantage of the previously developed natural graphical representation to recover viral phylogeny. Our results demonstrate that the proposed method is efficient and accurate for classifying viruses. The accuracy rates of our predictions such as for Baltimore II viruses are as high as 95.9% for family labels, 95.7% for subfamily labels and 96.5% for genus labels. Finally, we discover that proteomes lead to better viral classification when reliable protein sequences are abundant. In other cases, the accuracy rates using proteomes are still comparable to that of genomes.

This paper deals with the estimation of a high-dimensional covariance with a con- ditional sparsity structure and fast-diverging eigenvalues. By assuming sparse error covariance matrix in an approximate factor model, we allow for the presence of some cross-sectional correlation even after taking out common but unobservable factors. We introduce the Principal Orthogonal complEment Thresholding (POET) method to explore such an approximate factor structure with sparsity. The POET estimator includes the sample covariance matrix, the factor-based covariance matrix (Fan, Fan, and Lv, 2008), the thresholding estimator (Bickel and Levina, 2008) and the adaptive thresholding estimator (Cai and Liu, 2011) as specic examples. We provide mathe- matical insights when the factor analysis is approximately the same as the principal component analysis for high-dimensional data. The rates of convergence of the sparse residual covariance matrix and the conditional sparse covariance matrix are studied under various norms. It is shown that the impact of estimating the unknown factors vanishes as the dimensionality increases. The uniform rates of convergence for the un- observed factors and their factor loadings are derived. The asymptotic results are also veried by extensive simulation studies. Finally, a real data application on portfolio allocation is presented.

In deconvolution in R^d, d≥1, with mixing density p(∈\mathscr{P}) and kernel h, the mixture density f_p(∈\mathscr{F}_p) is estimated with MDE f_{\hat{p}n}, having upper L1-error rate, an, in probability or in risk; \hat{p}_n∈\mathscr{P}. In one application, \mathscr{P} consists of L1-separable densities in R with differences changing sign at most J times and h(x−y) Totally Positive. When h is known and p is \tilde{q}-smooth, vanishing outside a compact in R^d, plug-in upper bounds are provided for the L2-error rate of \hat{p}_n and its [s]-th mixed partial derivative \hat{p}^{(s)}_n, via ∥f_{\hat{p}_n}−f_p∥_1, with rates (log a^{−1}_n)^{−N_1} and a^{N_2}_n, respectively, for h super-smooth and smooth; \tilde{q}∈R^+, [s] ≤ \tilde{q}, d≥1, N_1>0, N_2>0. For a_n ∼ (logn)^ζ⋅(n^{−δ}), the former rate is optimal for any δ>0 and the latter misses the optimal by the factor (logn)^ξ when δ=.5; ζ>0, ξ>0. N_1 and N_2 appear in optimal rates and lower error and risk bounds in the deconvolution literature.

There is gained interest in understanding statistical inference under possibly non-sparse high-dimensional models. For a given component of the regression coefficient, we show that the difficulty of the problem depends on the sparsity of the corresponding row of the precision matrix of the covariates, not the sparsity of the regression coefficients. We develop new concepts of uniform and essentially uniform non-testability that allow the study of limitations of tests across a broad set of alternatives. Uniform non-testability identifies a collection of alternatives such that the power of any test, against any alternative in the group, is asymptotically at most equal to the nominal size of the test. Implications of the new constructions include new minimax testability results that in sharp contrast to the existing results, do not depend on the sparsity of the regression parameters. We identify new tradeoffs between testability and feature correlation. In particular, we show that in models with weak feature correlations minimax lower bound can be attained by a test whose power has the parametric rate regardless of the size of the model sparsity.