Imputation of truncated p-values for meta-analysis methods and its genomic application

TL;DR

This paper introduces three imputation methods to handle truncated p-values in meta-analysis, enabling more effective aggregation of genomic data when raw p-values are unavailable, and demonstrates their superiority over naive approaches.

Contribution

It develops and compares three novel imputation techniques for censored p-values in meta-analysis, extending evidence aggregation methods like Fisher's and Stouffer's.

Findings

Imputation methods outperform naive approaches in simulations.

Proposed methods effectively control false discovery rate.

Applications in genomic studies show improved detection of differentially expressed genes.

Abstract

Microarray analysis to monitor expression activities in thousands of genes simultaneously has become routine in biomedical research during the past decade. A tremendous amount of expression profiles are generated and stored in the public domain and information integration by meta-analysis to detect differentially expressed (DE) genes has become popular to obtain increased statistical power and validated findings. Methods that aggregate transformed $p$-value evidence have been widely used in genomic settings, among which Fisher's and Stouffer's methods are the most popular ones. In practice, raw data and $p$-values of DE evidence are often not available in genomic studies that are to be combined. Instead, only the detected DE gene lists under a certain $p$-value threshold (e.g., DE genes with $p$-value${}<0.001$) are reported in journal publications. The truncated $p$-value information makes the aforementioned meta-analysis methods inapplicable and researchers are forced to apply a less efficient vote counting method or na\"{i}vely drop the studies with incomplete information. The purpose of this paper is to develop effective meta-analysis methods for such situations with partially censored $p$-values. We developed and compared three imputation methods - mean imputation, single random imputation and multiple imputation - for a general class of evidence aggregation methods of which Fisher's and Stouffer's methods are special examples. The null distribution of each method was analytically derived and subsequent inference and genomic analysis frameworks were established. Simulations were performed to investigate the type I error, power and the control of false discovery rate (FDR) for (correlated) gene expression data. The proposed methods were applied to several genomic applications in colorectal cancer, pain and liquid association analysis of major depressive disorder (MDD). The results showed that imputation methods outperformed existing na\"{i}ve approaches. Mean imputation and multiple imputation methods performed the best and are recommended for future applications.