Evidence map›Paper›PMID 37018137›Full record

ArticleBioinformatics (Oxford, England)2023

Multiscale adaptive differential abundance analysis in microbial compositional data.

Shulei Wang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Profiling of endogenous metabolites and changes in intestinal microbiota distribution after GEN-001 (The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  6. Article
4 · The record

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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

1 author.

Shulei WangDepartment of Statistics, University of Illinois at Urbana-Champaign, Champaign, IL 61820, USA.ORCID 0000-0001-7440-9544

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationDifferential abundance analysis is an essential and commonly used tool to characterize the difference between microbial communities. However, identifying differentially abundant microbes remains a challenging problem because the observed microbiome data are inherently compositional, excessive sparse, and distorted by experimental bias. Besides these major challenges, the results of differential abundance analysis also depend largely on the choice of analysis unit, adding another practical complexity to this already complicated problem.

resultsIn this work, we introduce a new differential abundance test called the MsRDB test, which embeds the sequences into a metric space and integrates a multiscale adaptive strategy for utilizing spatial structure to identify differentially abundant microbes. Compared with existing methods, the MsRDB test can detect differentially abundant microbes at the finest resolution offered by data and provide adequate detection power while being robust to zero counts, compositional effect, and experimental bias in the microbial compositional dataset. Applications to both simulated and real microbial compositional datasets demonstrate the usefulness of the MsRDB test. AVAILABILITY AND IMPLEMENTATION: All analyses can be found under https://github.com/lakerwsl/MsRDB-Manuscript-Code.

Indexed as

Microbiota

Identifiers

PMID37018137
PMCPMC10112958

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.