Background: Measuring and understanding the function of the human microbiome is key for several aspects of health; however, the development of statistical methods specifically for the analysis of microbial gene expression (i.e., metatranscriptomics) is in its infancy. Many currently employed differential expression analysis methods have been designed for different data types and have not been evaluated in metatranscriptomics settings. To address this knowledge gap, we undertook a comprehensive evaluation and benchmarking of eight differential analysis methods for metatranscriptomics data.
Results: We used a combination of real and simulated metatranscriptomics data to evaluate the performance (i.e., model fit, Type-I error, and statistical power) of eights methods: log-normal (LN), logistic-beta (LB), MAST, Kruskal-Wallis, two-part Kruskal-Wallis, DESeq2, and ANCOM-BC and metagenomeSeq. The simulation was informed by supragingival biofilm microbiome data from about 300 preschool-age children enrolled in a study of early childhood caries (ECC), whereas validations were sought in two additional datasets, including an ECC and an inflammatory bowel disease one. The LB test showed the highest power in both small and large sample sizes and reasonably controlled Type-I error. Contrarily, MAST was hampered by inflated Type-I error. Using LN and LB tests, we found that genes C8PHV7 and C8PEV7, harbored by the lactate-producing Campylobacter gracilis, had the strongest association with ECC.
Conclusion: This comprehensive model evaluation findings offer practical guidance for the selection of appropriate methods for rigorous analyses of differential expression in metatranscriptomics data. Selection of an optimal method is likely to increase the possibility of detecting true signals while minimizing the chance of claiming false ones.
Differential expression analysis methods for ribonucleic acid-sequencing data