Evidence map›Paper›PMID 22536335›Full record

ArticlePloS one2012

Visualization and curve-parameter estimation strategies for efficient exploration of phenotype microarray kinetics.

Lea A I Vaas, Johannes Sikorski, Victoria Michael, Markus Göker, Hans-Peter Klenk

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

71 citing papers in PubMed.

  1. Longitudinal omics data analysis: approaches and applications.Computational and structural biotechnology journal · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Characteristics ofFrontiers in plant science · 2023
    Article
  6. Article
  7. Article
  8. Genotype-phenotype correlations within theFrontiers in microbiology · 2022
    Article
  9. International journal of systematic and evolutionary microbiology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Quantifying relative virulence: whenThe Journal of general virology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. International journal of systematic and evolutionary microbiology · 2020
    Article
  19. Article
  20. Microbial high throughput phenomics: The potential of an irreplaceable omics.Computational and structural biotechnology journal · 2020
    Review

11 more citing papers are in PubMed but not listed here.

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

5 authors.

Lea A I VaasDSMZ-German Collection for Microorganisms and Cell Cultures, Braunschweig, Germany.
Johannes Sikorski
Victoria Michael
Markus Göker
Hans-Peter Klenk

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Phenotype MicroArray (OmniLog® PM) system is able to simultaneously capture a large number of phenotypes by recording an organism's respiration over time on distinct substrates. This technique targets the object of natural selection itself, the phenotype, whereas previously addressed '-omics' techniques merely study components that finally contribute to it. The recording of respiration over time, however, adds a longitudinal dimension to the data. To optimally exploit this information, it must be extracted from the shapes of the recorded curves and displayed in analogy to conventional growth curves. METHODOLOGY: The free software environment R was explored for both visualizing and fitting of PM respiration curves. Approaches using either a model fit (and commonly applied growth models) or a smoothing spline were evaluated. Their reliability in inferring curve parameters and confidence intervals was compared to the native OmniLog® PM analysis software. We consider the post-processing of the estimated parameters, the optimal classification of curve shapes and the detection of significant differences between them, as well as practically relevant questions such as detecting the impact of cultivation times and the minimum required number of experimental repeats.

conclusionsWe provide a comprehensive framework for data visualization and parameter estimation according to user choices. A flexible graphical representation strategy for displaying the results is proposed, including 95% confidence intervals for the estimated parameters. The spline approach is less prone to irregular curve shapes than fitting any of the considered models or using the native PM software for calculating both point estimates and confidence intervals. These can serve as a starting point for the automated post-processing of PM data, providing much more information than the strict dichotomization into positive and negative reactions. Our results form the basis for a freely available R package for the analysis of PM data.

Indexed as

Data Interpretation, StatisticalPhenotypeSoftwareArea Under CurveComputer GraphicsConfidence IntervalsCulture MediaEnergy MetabolismEscherichia coliModels, BiologicalPseudomonas aeruginosaCulture Media

Identifiers

PMID22536335
PMCPMC3334903

What OpenQuestion holds

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LicenceCC BY
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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.