Evidence map›Paper›PMID 42867151›Full record

ArticleBioinformatics (Oxford, England)2026

Efficient and scalable Python implementation of ANCOM-BC and ANCOM-BC2 for omics differential abundance testing.

Zijun Wu, Huang Lin, James T Morton, Qiyun Zhu

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Zijun WuBiodesign Center for Fundamental and Applied Microbiomics, Arizona State University, Tempe, AZ 85281, United States.
Huang LinDepartment of Epidemiology and Biostatistics, School of Public Health, University of Maryland, College Park, MD 20742, United States.ORCID 0000-0002-4892-7871
James T MortonGutz Technologies, Inc., Covina, CA 91723, United States.
Qiyun ZhuBiodesign Center for Fundamental and Applied Microbiomics, Arizona State University, Tempe, AZ 85281, United States.

Funding

U.S. Department of Energy, Office of Science DE-SC0024320
6 · The paper itself

Abstract

summaryAnalysis of Compositions of Microbiomes with Bias Correction (ANCOM-BC) and its successor ANCOM-BC2 are critical algorithms for differential abundance analysis. Designed for handling compositional data, they feature the ability to estimate the unknown sampling fractions and correct the bias induced by their differences. While the original R package implementing the two methods is robust for standard dataset sizes, the increasing magnitude of modern multiomics studies presents computational challenges, often resulting in a runtime bottleneck for high-dimensional data. Here, we present native Python implementations of both ANCOM-BC and ANCOM-BC2 in the scikit-bio package, significantly accelerating the workflow and enabling their application to large-scale datasets. By leveraging vectorization with NumPy and numerical optimization in SciPy, we enhanced the efficiency of both methods without compromising their statistical accuracy. The benchmarking results revealed a dramatic increase in performance in both simulated and real datasets. We demonstrated that our Python implementations generated test results matching the original R code, while achieving 380- and 147-fold faster runtimes and 97.4% and 96.2% lower memory consumption on the largest tested dataset, respectively. The Python implementations allow for the analysis of datasets that are significantly larger than previously possible, and enable applications to alternative omics data types and complex statistical models that vary greatly by the number of samples, features, and covariates. AVAILABILITY AND IMPLEMENTATION: https://github.com/scikit-bio/scikit-bio.

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Computational BiologyMicrobiotaSoftwareAlgorithmsMultiomics

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.