bioRxivMicrobiology
Zero is not absence: censoring-based differential abundance analysis for microbiome data
Abstract
Microbiome data analysis faces the challenge of sparsity, with many entries recorded as zeros. In differential abundance analysis, the presence of excessive zeros in data violates distributional assumptions and creates ties, leading to an increased risk of type I errors and reduced statistical power. To address this, we developed a novel normalization method, called CAMP, for microbiome data by treating zeros as censored observations, transforming raw read counts into tie-free time-to-event-like data. This enables the use of survival analysis techniques, like the Cox proportional hazards model, for differential abundance analysis. Extensive simulations demonstrate that CAMP achieves proper type I error control and high power. Applying CAMP to a human gut microbiome dataset, we identify 60 new differentially abundant taxa across geographic locations, showcasing its usefulness. CAMP over-comes sparsity challenges, enabling improved statistical analysis and providing valuable insights into microbiome data in various contexts.
- organism: human
- assay: metagenomics
- research focus: differential expression
- approach: statistical model
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