Evidence map›Paper›PMID 27864351›Full record

ArticleGenome research2017

Detecting differential growth of microbial populations with Gaussian process regression.

Peter D Tonner, Cynthia L Darnell, Barbara E Engelhardt, Amy K Schmid

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
  2. Article
  3. Stochasticity in mammalian cell growth rates drives cell-to-cell variability independently of cell size and divisions.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Heterotrophic Selenium Incorporation intoFoods (Basel, Switzerland) · 2024
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  13. Systems biology approach to functionally assess theProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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  18. Quantifying relative virulence: whenThe Journal of general virology · 2021
    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

4 authors at 2 institutions in 1 country.

Peter D TonnerProgram in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina 27708, USA.
Cynthia L DarnellBiology Department, Duke University, Durham, North Carolina 27708, USA.
Barbara E EngelhardtComputer Science Department, Center for Statistics and Machine Learning, Princeton University, Princeton, New Jersey 08540, USA.
Amy K SchmidProgram in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina 27708, USA.
Duke University · USPrinceton University · US

Funding

Identification and validation of cell specific eQTLs by Bayesian modelingR01MH101822 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BROWN, CHRISTOPHER DAVID, ENGELHARDT, BARBARA · 2013 to 2016
$1.9M
Statistical models to investigate long-distance QTL transcription regulationR00HG006265 · NHGRI · PRINCETON UNIVERSITY · PI ENGELHARDT, BARBARA · 2012 to 2014
$747k
NHGRI NIH HHS R00 HG006265NIMH NIH HHS R01 MH101822
6 · The paper itself

Abstract

Microbial growth curves are used to study differential effects of media, genetics, and stress on microbial population growth. Consequently, many modeling frameworks exist to capture microbial population growth measurements. However, current models are designed to quantify growth under conditions for which growth has a specific functional form. Extensions to these models are required to quantify the effects of perturbations, which often exhibit nonstandard growth curves. Rather than assume specific functional forms for experimental perturbations, we developed a general and robust model of microbial population growth curves using Gaussian process (GP) regression. GP regression modeling of high-resolution time-series growth data enables accurate quantification of population growth and allows explicit control of effects from other covariates such as genetic background. This framework substantially outperforms commonly used microbial population growth models, particularly when modeling growth data from environmentally stressed populations. We apply the GP growth model and develop statistical tests to quantify the differential effects of environmental perturbations on microbial growth across a large compendium of genotypes in archaea and yeast. This method accurately identifies known transcriptional regulators and implicates novel regulators of growth under standard and stress conditions in the model archaeal organism Halobacterium salinarum For yeast, our method correctly identifies known phenotypes for a diversity of genetic backgrounds under cyclohexamide stress and also detects previously unidentified oxidative stress sensitivity across a subset of strains. Together, these results demonstrate that the GP models are interpretable, recapitulating biological knowledge of growth response while providing new insights into the relevant parameters affecting microbial population growth.

Indexed as

Models, BiologicalHalobacterium salinarumNormal DistributionPhenotypeYeasts

Identifiers

PMID27864351
PMCPMC5287237
OpenAlexW2554987818

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.