Abstract
Microbiome studies often seek to determine how the absolute abundances of individual taxa change across biological conditions, yet sequencing read counts are sample-specific scaled representations of those abundances. Because sampling depth can differ across samples, fold changes calculated directly from sequencing read counts do not generally represent absolute-abundance fold changes. Normalization methods attempt to account for these between-sample differences in sampling depth, but their accuracy depends on the reference used. In particular, total-sum scaling uses all taxa as the reference and can introduce compositional bias. Reference-based methods instead rely on taxa that are stable across conditions, but contamination of the reference set by differentially abundant (DA) taxa can distort sampling-depth estimation and downstream inference. Here, we present iterative reference selection (IRS), a robust normalization method that iteratively screens and refines a candidate reference set to exclude DA taxa. By deriving a clean reference set, IRS accurately captures between-sample differences in sampling depth and recovers absolute-abundance fold changes. Benchmarking using simulations and datasets with experimental absolute quantification shows that IRS outperforms standard scaling and existing reference-based methods in controlling false discovery rates while maintaining power.
| Original language | English |
|---|---|
| Article number | bbag495 |
| Journal | Briefings in Bioinformatics |
| Volume | 27 |
| Issue number | 5 |
| DOIs | |
| State | Published - Sep 2026 |
Keywords
- bioinformatics
- differential abundance
- microbiome
- normalization
Fingerprint
Dive into the research topics of 'IRS: iterative reference selection improves normalization of microbiome sequencing data'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver