Evidence map›Paper›PMID 24586794›Full record

ArticlePloS one2014

A developmental approach to predicting neuronal connectivity from small biological datasets: a gradient-based neuron growth model.

Roman Borisyuk, Abul Kalam Al Azad, Deborah Conte, Alan Roberts, Stephen R Soffe

Open access · goldAbstract read
In one paragraph

Article in PloS one, 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
2.2field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Mechanisms Underlying the Recruitment of Inhibitory Interneurons in Fictive Swimming in DevelopingThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Generative models for network neuroscience: prospects and promise.Journal of the Royal Society, Interface · 2017
    Review
  10. Article
  11. Article
  12. Article
  13. The generation of antiphase oscillations and synchrony by a rebound-based vertebrate central pattern generator.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    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

5 authors at 3 institutions in 2 countries.

Roman BorisyukSchool of Computing and Mathematics, Plymouth University, Plymouth, United Kingdom ; Institute of Mathematical Problems in Biology of the Russian Academy of Sciences, Pushchino, Russia.
Abul Kalam Al AzadSchool of Computing and Mathematics, Plymouth University, Plymouth, United Kingdom.
Deborah ConteSchool of Biological Sciences, University of Bristol, Bristol, United Kingdom.
Alan RobertsSchool of Biological Sciences, University of Bristol, Bristol, United Kingdom.
Stephen R SoffeSchool of Biological Sciences, University of Bristol, Bristol, United Kingdom.
University of Bristol · GBInstitute of Mathematical Problems of Biology · RUUniversity of Plymouth · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G006369/1Biotechnology and Biological Sciences Research Council BB/G006652/1
6 · The paper itself

Abstract

Relating structure and function of neuronal circuits is a challenging problem. It requires demonstrating how dynamical patterns of spiking activity lead to functions like cognitive behaviour and identifying the neurons and connections that lead to appropriate activity of a circuit. We apply a "developmental approach" to define the connectome of a simple nervous system, where connections between neurons are not prescribed but appear as a result of neuron growth. A gradient based mathematical model of two-dimensional axon growth from rows of undifferentiated neurons is derived for the different types of neurons in the brainstem and spinal cord of young tadpoles of the frog Xenopus. Model parameters define a two-dimensional CNS growth environment with three gradient cues and the specific responsiveness of the axons of each neuron type to these cues. The model is described by a nonlinear system of three difference equations; it includes a random variable, and takes specific neuron characteristics into account. Anatomical measurements are first used to position cell bodies in rows and define axon origins. Then a generalization procedure allows information on the axons of individual neurons from small anatomical datasets to be used to generate larger artificial datasets. To specify parameters in the axon growth model we use a stochastic optimization procedure, derive a cost function and find the optimal parameters for each type of neuron. Our biologically realistic model of axon growth starts from axon outgrowth from the cell body and generates multiple axons for each different neuron type with statistical properties matching those of real axons. We illustrate how the axon growth model works for neurons with axons which grow to the same and the opposite side of the CNS. We then show how, by adding a simple specification for dendrite morphology, our model "developmental approach" allows us to generate biologically-realistic connectomes.

Indexed as

Models, NeurologicalAnimalsAxonsNerve NetNeurogenesisNeuronsSpinal CordXenopus

Identifiers

PMID24586794
PMCPMC3931784
OpenAlexW2002392529

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.