Evidence map›Paper›PMID 24447135›Full record

ArticleBioTechniques2014

Quantitative analysis of colony morphology in yeast.

Pekka Ruusuvuori, Jake Lin, Adrian C Scott, Zhihao Tan, Saija Sorsa, Aleksi Kallio, Matti Nykter, Olli Yli-Harja, Ilya Shmulevich, Aimée M Dudley

Abstract read
In one paragraph

Article in BioTechniques, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

10 authors.

Pekka RuusuvuoriDepartment of Signal Processing, Tampere University of Technology, Tampere, Finland; Institute for Systems Biology, Seattle, WA.
Jake LinDepartment of Signal Processing, Tampere University of Technology, Tampere, Finland; Institute for Systems Biology, Seattle, WA; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg.
Adrian C ScottPacific Northwest Diabetes Research Institute, Seattle, WA.
Zhihao TanPacific Northwest Diabetes Research Institute, Seattle, WA; Molecular and Cellular Biology Program, University of Washington, Seattle, WA.
Saija SorsaDepartment of Signal Processing, Tampere University of Technology, Tampere, Finland.
Aleksi KallioInstitute of Biomedical Technology, University of Tampere, Tampere, Finland.
Matti NykterInstitute of Biomedical Technology, University of Tampere, Tampere, Finland.
Olli Yli-HarjaDepartment of Signal Processing, Tampere University of Technology, Tampere, Finland; Institute for Systems Biology, Seattle, WA.
Ilya ShmulevichDepartment of Signal Processing, Tampere University of Technology, Tampere, Finland; Institute for Systems Biology, Seattle, WA.
Aimée M DudleyPacific Northwest Diabetes Research Institute, Seattle, WA; Molecular and Cellular Biology Program, University of Washington, Seattle, WA.

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI BALIGA, NITIN S · 2006 to 2016
$30.6M
NIGMS NIH HHS P50 GM076547
6 · The paper itself

Abstract

Microorganisms often form multicellular structures such as biofilms and structured colonies that can influence the organism's virulence, drug resistance, and adherence to medical devices. Phenotypic classification of these structures has traditionally relied on qualitative scoring systems that limit detailed phenotypic comparisons between strains. Automated imaging and quantitative analysis have the potential to improve the speed and accuracy of experiments designed to study the genetic and molecular networks underlying different morphological traits. For this reason, we have developed a platform that uses automated image analysis and pattern recognition to quantify phenotypic signatures of yeast colonies. Our strategy enables quantitative analysis of individual colonies, measured at a single time point or over a series of time-lapse images, as well as the classification of distinct colony shapes based on image-derived features. Phenotypic changes in colony morphology can be expressed as changes in feature space trajectories over time, thereby enabling the visualization and quantitative analysis of morphological development. To facilitate data exploration, results are plotted dynamically through an interactive Yeast Image Analysis web application (YIMAA; http://yimaa.cs.tut.fi) that integrates the raw and processed images across all time points, allowing exploration of the image-based features and principal components associated with morphological development.

Indexed as

Image Processing, Computer-AssistedSoftwareAlgorithmsInternetSaccharomyces cerevisiaecolony morphologyimage analysisphenotypesoftwaretime-lapseyeast

Identifiers

PMID24447135
PMCPMC3996921

What OpenQuestion holds

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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.