Evidence map›Paper›PMID 27851808›Full record

ArticlePloS one2016

An Observation-Driven Agent-Based Modeling and Analysis Framework for C. elegans Embryogenesis.

Zi Wang, Benjamin J Ramsey, Dali Wang, Kwai Wong, Husheng Li, Eric Wang, Zhirong Bao

Abstract read
In one paragraph

Article in PloS one, 2016. 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
–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

6 citing papers in PubMed.

  1. Article
  2. Analysis of developmental gene expression using smFISH andbioRxiv : the preprint server for biology · 2024
    Article
  3. Article
  4. Review
  5. 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.

Zi WangDepartment of Electrical Engineering and Computer Science, University of Tennessee, Knoxville, Tennessee, United States of America.
Benjamin J RamseyJoint Institute for Computational Sciences, University of Tennessee, Knoxville, Tennessee, United States of America.
Dali WangClimate Change Science Institute, Oak Ridge National Laboratory, Oak Ridge, Tennessee, United States of America.
Kwai WongJoint Institute for Computational Sciences, University of Tennessee, Knoxville, Tennessee, United States of America.
Husheng LiDepartment of Electrical Engineering and Computer Science, University of Tennessee, Knoxville, Tennessee, United States of America.
Eric WangFarragut High School, Knoxville, Tennessee, United States of America.
Zhirong BaoDevelopmental Biology Program, Sloan Kettering Institute, New York City, New York, United States of America.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
The Ubiquitin-Proteasome System in Metazoan EmbryogenesisR01GM097576 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI BAO, ZHIRONG · 2011 to 2020
$3.3M
NCI NIH HHS P30 CA008748NIGMS NIH HHS R01 GM097576
6 · The paper itself

Abstract

With cutting-edge live microscopy and image analysis, biologists can now systematically track individual cells in complex tissues and quantify cellular behavior over extended time windows. Computational approaches that utilize the systematic and quantitative data are needed to understand how cells interact in vivo to give rise to the different cell types and 3D morphology of tissues. An agent-based, minimum descriptive modeling and analysis framework is presented in this paper to study C. elegans embryogenesis. The framework is designed to incorporate the large amounts of experimental observations on cellular behavior and reserve data structures/interfaces that allow regulatory mechanisms to be added as more insights are gained. Observed cellular behaviors are organized into lineage identity, timing and direction of cell division, and path of cell movement. The framework also includes global parameters such as the eggshell and a clock. Division and movement behaviors are driven by statistical models of the observations. Data structures/interfaces are reserved for gene list, cell-cell interaction, cell fate and landscape, and other global parameters until the descriptive model is replaced by a regulatory mechanism. This approach provides a framework to handle the ongoing experiments of single-cell analysis of complex tissues where mechanistic insights lag data collection and need to be validated on complex observations.

Indexed as

Embryonic DevelopmentSystems AnalysisAnimalsCaenorhabditis elegansCell CountCell CycleCell LineageCell MovementComputer SimulationEmbryo, NonmammalianModels, BiologicalReproducibility of Results

Identifiers

PMID27851808
PMCPMC5113041

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.