Permutation $p$-value approximation via generalized Stolarsky invariance
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It is common for genomic data analysis to use $p$-values from a large number of permutation tests. The multiplicity of tests may require very tiny $p$-values in order to reject any null hypotheses and the common practice of using randomly sampled permutations then becomes very expensive. We propose an inexpensive approximation to $p$-values for two sample linear test statistics, derived from Stolarsky’s invariance principle. The method creates a geometrically derived reference set of approximate $p$-values for each hypothesis. The average of that set is used as a point estimate $\hat{p}$ and our generalization of the invariance principle allows us to compute the variance of the $p$-values in that set. We find that in cases where the point estimate is small, the variance is a modest multiple of the square of that point estimate, yielding a relative error property similar to that of saddlepoint approximations. On a Parkinson’s disease data set, the new approximation is faster and more accurate than the saddlepoint approximation. We also obtain a simple probabilistic explanation of Stolarsky’s invariance principle.
In this paper, we develop bootstrap methods for factor-augmented regressions with potentially weak common components, allowing signal eigenvalues to diverge at heterogeneous rates $N^{α_k}$, where $0<α_k\leq1$, $k=1,\ldots,r$. The regression estimator targets a rotation of the latent parameter vector that may be data dependent, while factor estimation can induce asymptotic bias. The proposed procedure directly constructs the rotation-specific target in the bootstrap world,…
Normality pre-tests on reduced-form innovations cannot detect whether two or more underlying structural shocks are Gaussian, and hence cannot detect a failure of identification in non-Gaussian SVARs. We propose a bootstrap-based approach that reveals such a failure. Under the null of valid identification and certain regularity conditions, the conditional bootstrap distribution of the maximum likelihood estimator of the impact matrix is asymptotically normal, so the…
Motivation: Mediation analysis is an important tool for elucidating causal mechanisms in biomedical research and has recently gained increasing attention in microbiome studies. Motivated by a microbiome study of acute myeloid leukemia (AML) patients, we investigate whether the effect of induction chemotherapy intensity on infection status is mediated through gut microbial taxa. This problem poses substantial methodological challenges due to the high dimensionality, zero…
I study randomization inference for dynamic causal effects in panels with many units and few periods when treatment is endogenous and an instrument is as good as randomly assigned only through the innovations of a first-order autoregressive assignment mechanism with unknown persistence. The persistence is a nuisance parameter in two senses: it determines which weighted average of heterogeneous causal effects the instrumented local projection estimand measures, and it governs…
Two frequent approaches for identifying structural VARs are external instruments, which carry economic content but are often weak, and non-Gaussianity of the shocks, which provides statistical identification but carries no economic meaning. We combine the two strategies in a single generalized method of moments framework. This hybrid approach point-identifies the target shocks while also identifying the non-target shocks up to sign and ordering. Under suitable rank…
多层主效应矩阵因子模型
We propose a multilevel main effects matrix factor model (MMEFM) to extract meaningful row and column effects from groups of matrix data. As a generalization of a multilevel matrix factor model, we provide rigorous definitions of MMEFM and identifications, together with iterative algorithms for the estimators of all global and local components in the main effects and common component, including global/local main effects and core ranks, with rates of convergence spelt out. An…