Evidence map›Paper›PMID 39936028›Full record

ArticleArXiv2024

Group-wise normalization in differential abundance analysis of microbiome samples.

Dylan Clark-Boucher, Brent Coull, Harrison T Reeder, Fenglei Wang, Qi Sun, Jacqueline R Starr, Kyu Ha Lee

Abstract readPreprint
In one paragraph

Article in ArXiv, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Dylan Clark-BoucherDepartment of Biostatistics, Harvard TH Chan School of Public Health, Boston, MA, United States.
Brent CoullDepartment of Biostatistics, Harvard TH Chan School of Public Health, Boston, MA, United States.
Harrison T ReederBiostatistics, Massachusetts General Hospital, Boston, MA, United States.
Fenglei WangDepartment of Nutrition, Harvard TH Chan School of Public Health, Boston, MA, United States.
Qi SunDepartment of Nutrition, Harvard TH Chan School of Public Health, Boston, MA, United States.
Jacqueline R StarrChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, United States.
Kyu Ha LeeDepartment of Biostatistics, Harvard TH Chan School of Public Health, Boston, MA, United States.

Funding

PHACS - Data and Operations CenterU01HD052102 · NICHD · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI WILLIAMS, PAIGE L · 2005 to 2019
$242.7M
The Adolescent Master Protocol (AMP) Up Series ProjectP01HD103133 · NICHD · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI CHADWICK, ELLEN GOULD, HERNANDEZ-DIAZ, SONIA · 2020 to 2024
$88.3M
Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI JAIME ELIZABETH HART · 1985 to 2026
$44.6M
Life Course Cancer Epidemiology Cohort in WomenU01CA176726 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI ELIASSEN, A. HEATHER, WILLETT, WALTER C. · 2018 to 2025
$22.4M
Cancer Epidemiology Cohort in Male Health ProfessionalsU01CA167552 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Lorelei Mucci, Walter C. Willett · 2017 to 2026
$17.0M
Pediatric HIV/AIDS Cohort Study (PHACS): Understanding Maternal HIV Disease through Pregnancy and the Postpartum Period and its Role in Child Health OutcomesU01HD052104 · NICHD · TULANE UNIVERSITY OF LOUISIANA · PI VAN DYKE, RUSSELL B. · 2005 to 2019
$15.7M
Interdisciplinary training: Statistical Genetics/Genomics and Computational BiologyT32GM135117 · NIGMS · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Curtis Huttenhower, XIHONG LIN · 2020 to 2026
$3.1M
Bayesian multivariate 3D spatial modeling for microbiome image analysisR01GM126257 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, KYU HA, STARR, JACQUELINE R · 2021 to 2024
$2.4M
Multivariate Bayesian variable selection for high-dimensional oral microbiome dataR03DE027486 · NIDCR · HARVARD SCHOOL OF PUBLIC HEALTH · PI LEE, KYU HA · 2018 to 2019
$382k
NCI NIH HHS U01 CA167552NCI NIH HHS U01 CA176726NICHD NIH HHS P01 HD103133NICHD NIH HHS U01 HD052102NICHD NIH HHS U01 HD052104NIDCR NIH HHS R03 DE027486NIEHS NIH HHS P30 ES000002NIGMS NIH HHS R01 GM126257NIGMS NIH HHS T32 GM135117
6 · The paper itself

Abstract

Motivation: A key challenge in differential abundance analysis of microbial samples is that the counts for each sample are compositional, resulting in biased comparisons of the absolute abundance across study groups. Normalization-based differential abundance analysis methods rely on external normalization factors that account for the compositionality by standardizing the counts onto a common numerical scale. However, existing normalization methods have struggled at maintaining the false discovery rate in settings where the variance or compositional bias is large. This article proposes a novel framework for normalization that can reduce bias in differential abundance analysis by re-conceptualizing normalization as a group-level task. We present two normalization methods within the group-wise framework: group-wise relative log expression (G-RLE) and fold-truncated sum scaling (FTSS). Results: G-RLE and FTSS achieve higher statistical power for identifying differentially abundant taxa than existing methods in model-based and synthetic data simulation settings, while maintaining the false discovery rate in challenging scenarios where existing methods suffer. The best results are obtained from using FTSS normalization with the differential abundance analysis method MetagenomeSeq. Availability and Implementation: Code for implementing the methods and replicating the analysis can be found at our GitHub page.

Identifiers

PMID39936028
PMCPMC11812596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.