Evidence map›Paper›PMID 34823466›Full record

ArticleBMC bioinformatics2021

Randomized quantile residuals for diagnosing zero-inflated generalized linear mixed models with applications to microbiome count data.

Wei Bai, Mei Dong, Longhai Li, Cindy Feng, Wei Xu

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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 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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  4. deMULTIplex2: robust sample demultiplexing for scRNA-seq.bioRxiv : the preprint server for biology · 2023
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5 · Who and what money

Authors and funding

5 authors.

Wei Bai *Department of Mathematics and Statistics, University of Saskatchewan, Saskatoon, CA, Canada.
Mei Dong *Dalla Lana School of Public Health, University of Toronto, Toronto, CA, Canada.
Longhai LiDepartment of Mathematics and Statistics, University of Saskatchewan, Saskatoon, CA, Canada. longhai.li@usask.ca.
Cindy FengDepartment of Community Health and Epidemiology, Dalhousie University, Halifax, CA, Canada.
Wei XuDalla Lana School of Public Health, University of Toronto, Toronto, CA, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor differential abundance analysis, zero-inflated generalized linear models, typically zero-inflated NB models, have been increasingly used to model microbiome and other sequencing count data. A common assumption in estimating the false discovery rate is that the p values are uniformly distributed under the null hypothesis, which demands that the postulated model fit the count data adequately. Mis-specification of the distribution of the count data may lead to excess false discoveries. Therefore, model checking is critical to control the FDR at a nominal level in differential abundance analysis. Increasing studies show that the method of randomized quantile residual (RQR) performs well in diagnosing count regression models. However, the performance of RQR in diagnosing zero-inflated GLMMs for sequencing count data has not been extensively investigated in the literature.

resultsWe conduct large-scale simulation studies to investigate the performance of the RQRs for zero-inflated GLMMs. The simulation studies show that the type I error rates of the GOF tests with RQRs are very close to the nominal level; in addition, the scatter-plots and Q-Q plots of RQRs are useful in discerning the good and bad models. We also apply the RQRs to diagnose six GLMMs to a real microbiome dataset. The results show that the OTU counts at the genus level of this dataset (after a truncation treatment) can be modelled well by zero-inflated and zero-modified NB models.

conclusionRQR is an excellent tool for diagnosing GLMMs for zero-inflated count data, particularly the sequencing count data arising in microbiome studies. In the supplementary materials, we provided two generic R functions, called rqr.glmmtmb and rqr.hurdle.glmmtmb, for calculating the RQRs given fitting outputs of the R package glmmTMB.

Indexed as

MicrobiotaModels, StatisticalComputer SimulationLinear ModelsPoisson DistributionResearch Design

Identifiers

PMID34823466
PMCPMC8620156

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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.