Evidence map›Paper›PMID 34229628›Full record

ArticleBMC bioinformatics2021

Feature selection and causal analysis for microbiome studies in the presence of confounding using standardization.

Emily Goren, Chong Wang, Zhulin He, Amy M Sheflin, Dawn Chiniquy, Jessica E Prenni, Susannah Tringe, Daniel P Schachtman, Peng Liu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. IBD Subtype-RegulatorsFrontiers in pharmacology · 2022
    Article
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

9 authors.

Emily GorenDepartment of Statistics, Iowa State University, 2438 Osborn Dr, Ames, IA, 50011, USA.ORCID http://orcid.org/0000-0002-0202-5856
Chong WangDepartment of Statistics, Iowa State University, 2438 Osborn Dr, Ames, IA, 50011, USA.
Zhulin HeDepartment of Statistics, Iowa State University, 2438 Osborn Dr, Ames, IA, 50011, USA.
Amy M SheflinDepartment of Horticulture and Landscape Architecture, Colorado State University, 301 University Ave, Fort Collins, CO, 80523, USA.
Dawn ChiniquyDepartment of Energy, Joint Genome Institute, 2800 Mitchell Dr, Walnut Creek, CA, 94598, USA.
Jessica E PrenniDepartment of Horticulture and Landscape Architecture, Colorado State University, 301 University Ave, Fort Collins, CO, 80523, USA.
Susannah TringeDepartment of Energy, Joint Genome Institute, 2800 Mitchell Dr, Walnut Creek, CA, 94598, USA.
Daniel P SchachtmanDepartment of Agronomy and Horticulture, University of Nebraska, 1825 N 38th St, Lincoln, NE, 68583, USA.
Peng LiuDepartment of Statistics, Iowa State University, 2438 Osborn Dr, Ames, IA, 50011, USA. pliu@iastate.edu.ORCID http://orcid.org/0000-0002-2093-8018

Funding

U.S. Department of Energy DE-SC0014395
6 · The paper itself

Abstract

backgroundMicrobiome studies have uncovered associations between microbes and human, animal, and plant health outcomes. This has led to an interest in developing microbial interventions for treatment of disease and optimization of crop yields which requires identification of microbiome features that impact the outcome in the population of interest. That task is challenging because of the high dimensionality of microbiome data and the confounding that results from the complex and dynamic interactions among host, environment, and microbiome. In the presence of such confounding, variable selection and estimation procedures may have unsatisfactory performance in identifying microbial features with an effect on the outcome.

resultsIn this manuscript, we aim to estimate population-level effects of individual microbiome features while controlling for confounding by a categorical variable. Due to the high dimensionality and confounding-induced correlation between features, we propose feature screening, selection, and estimation conditional on each stratum of the confounder followed by a standardization approach to estimation of population-level effects of individual features. Comprehensive simulation studies demonstrate the advantages of our approach in recovering relevant features. Utilizing a potential-outcomes framework, we outline assumptions required to ascribe causal, rather than associational, interpretations to the identified microbiome effects. We conducted an agricultural study of the rhizosphere microbiome of sorghum in which nitrogen fertilizer application is a confounding variable. In this study, the proposed approach identified microbial taxa that are consistent with biological understanding of potential plant-microbe interactions.

conclusionsStandardization enables more accurate identification of individual microbiome features with an effect on the outcome of interest compared to other variable selection and estimation procedures when there is confounding by a categorical variable.

Indexed as

MicrobiotaAnimalsConfounding Factors, EpidemiologicHumansPlantsReference StandardsRhizosphereCausal inferenceHigh-dimensional feature selectionMicrobiome analysisNext-generation sequencingStandardization

Identifiers

PMID34229628
PMCPMC8261956

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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.