Evidence map›Paper›PMID 35584140›Full record

ArticlePLoS computational biology2022

CBEA: Competitive balances for taxonomic enrichment analysis.

Quang P Nguyen, Anne G Hoen, H Robert Frost

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 42% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Quang P NguyenDepartment of Biomedical Data Science, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire, United States of America.ORCID 0000-0002-2072-3279
Anne G HoenDepartment of Biomedical Data Science, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire, United States of America.
H Robert FrostDepartment of Biomedical Data Science, Geisel School of Medicine at Dartmouth College, Hanover, New Hampshire, United States of America.ORCID 0000-0002-6794-9945
Dartmouth College · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
Zhao - Proj 2P20GM130454 · NIGMS · DARTMOUTH COLLEGE · PI Li Song · 2019 to 2026
$27.2M
Multi-omic Functional Integration Using NetworksR01LM012723 · NLM · DARTMOUTH COLLEGE · PI HOEN, ANNE GATEWOOD · 2017 to 2020
$1.4M
Cancer-specific gene set testingR21CA253408 · NCI · DARTMOUTH COLLEGE · PI FROST, HILDRETH · 2020 to 2020
$451k
NCI NIH HHS P30 CA023108NCI NIH HHS R21 CA253408NIGMS NIH HHS P20 GM130454NLM NIH HHS R01 LM012723
6 · The paper itself

Abstract

Research in human-associated microbiomes often involves the analysis of taxonomic count tables generated via high-throughput sequencing. It is difficult to apply statistical tools as the data is high-dimensional, sparse, and compositional. An approachable way to alleviate high-dimensionality and sparsity is to aggregate variables into pre-defined sets. Set-based analysis is ubiquitous in the genomics literature and has demonstrable impact on improving interpretability and power of downstream analysis. Unfortunately, there is a lack of sophisticated set-based analysis methods specific to microbiome taxonomic data, where current practice often employs abundance summation as a technique for aggregation. This approach prevents comparison across sets of different sizes, does not preserve inter-sample distances, and amplifies protocol bias. Here, we attempt to fill this gap with a new single-sample taxon enrichment method that uses a novel log-ratio formulation based on the competitive null hypothesis commonly used in the enrichment analysis literature. Our approach, titled competitive balances for taxonomic enrichment analysis (CBEA), generates sample-specific enrichment scores as the scaled log-ratio of the subcomposition defined by taxa within a set and the subcomposition defined by its complement. We provide sample-level significance testing by estimating an empirical null distribution of our test statistic with valid p-values. Herein, we demonstrate, using both real data applications and simulations, that CBEA controls for type I error, even under high sparsity and high inter-taxa correlation scenarios. Additionally, CBEA provides informative scores that can be inputs to downstream analyses such as prediction tasks.

Indexed as

MicrobiotaGenomicsHigh-Throughput Nucleotide SequencingHumans

Identifiers

PMID35584140
PMCPMC9154102
OpenAlexW4280534380

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.