Evidence map›Paper›PMID 25816290›Full record

ArticlePloS one2015

Model-independent phenotyping of C. elegans locomotion using scale-invariant feature transform.

Yelena Koren, Raphael Sznitman, Paulo E Arratia, Christopher Carls, Predrag Krajacic, André E X Brown, Josué Sznitman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 32% of its field
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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Powerful and interpretable behavioural features for quantitative phenotyping ofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Article
  6. 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

7 authors at 5 institutions in 4 countries.

Yelena KorenDepartment of Biomedical Engineering, Technion-Israel Institute of Technology, Israel.
Raphael SznitmanOphthalmic Technology Group, ARTORG Center, University of Bern, Switzerland.
Paulo E ArratiaDepartment of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia PA, USA.
Christopher CarlsDepartment of Biomedical Sciences, West Virginia School of Osteopathic Medicine, Lewisburg WV, USA.
Predrag KrajacicDepartment of Biomedical Sciences, West Virginia School of Osteopathic Medicine, Lewisburg WV, USA.
André E X BrownMRC Clinical Sciences Centre, Faculty of Medicine, Imperial College London, UK.
Josué SznitmanDepartment of Biomedical Engineering, Technion-Israel Institute of Technology, Israel.
Technion – Israel Institute of Technology · ILWest Virginia School of Osteopathic Medicine · USImperial College London · GBUniversity of Bern · CHUniversity of Pennsylvania · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

To uncover the genetic basis of behavioral traits in the model organism C. elegans, a common strategy is to study locomotion defects in mutants. Despite efforts to introduce (semi-)automated phenotyping strategies, current methods overwhelmingly depend on worm-specific features that must be hand-crafted and as such are not generalizable for phenotyping motility in other animal models. Hence, there is an ongoing need for robust algorithms that can automatically analyze and classify motility phenotypes quantitatively. To this end, we have developed a fully-automated approach to characterize C. elegans' phenotypes that does not require the definition of nematode-specific features. Rather, we make use of the popular computer vision Scale-Invariant Feature Transform (SIFT) from which we construct histograms of commonly-observed SIFT features to represent nematode motility. We first evaluated our method on a synthetic dataset simulating a range of nematode crawling gaits. Next, we evaluated our algorithm on two distinct datasets of crawling C. elegans with mutants affecting neuromuscular structure and function. Not only is our algorithm able to detect differences between strains, results capture similarities in locomotory phenotypes that lead to clustering that is consistent with expectations based on genetic relationships. Our proposed approach generalizes directly and should be applicable to other animal models. Such applicability holds promise for computational ethology as more groups collect high-resolution image data of animal behavior.

Indexed as

PhenotypeAlgorithmsAnimalsBiomechanical PhenomenaCaenorhabditis elegansLocomotionModels, Animal

Identifiers

PMID25816290
PMCPMC4376858
OpenAlexW1977443240

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.