Evidence map›Paper›PMID 26147508›Full record

ArticlePloS one2015

A Computational Framework for Bioimaging Simulation.

Masaki Watabe, Satya N V Arjunan, Seiya Fukushima, Kazunari Iwamoto, Jun Kozuka, Satomi Matsuoka, Yuki Shindo, Masahiro Ueda, Koichi Takahashi

Abstract 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Simulated single molecule microscopy with SMeagol.Bioinformatics (Oxford, England) · 2016
    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

9 authors.

Masaki WatabeLaboratory for Biochemical Simulation, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Satya N V ArjunanLaboratory for Biochemical Simulation, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Seiya FukushimaLaboratory for Cell Signaling Dynamics, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan; Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Kazunari IwamotoLaboratory for Biochemical Simulation, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Jun KozukaLaboratory for Cell Signaling Dynamics, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Satomi MatsuokaLaboratory for Cell Signaling Dynamics, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan.
Yuki ShindoLaboratory for Biochemical Simulation, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan; Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Masahiro UedaLaboratory for Cell Signaling Dynamics, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan; Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Koichi TakahashiLaboratory for Biochemical Simulation, Quantitative Biology Center, RIKEN, Suita, Osaka, Japan; Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using bioimaging technology, biologists have attempted to identify and document analytical interpretations that underlie biological phenomena in biological cells. Theoretical biology aims at distilling those interpretations into knowledge in the mathematical form of biochemical reaction networks and understanding how higher level functions emerge from the combined action of biomolecules. However, there still remain formidable challenges in bridging the gap between bioimaging and mathematical modeling. Generally, measurements using fluorescence microscopy systems are influenced by systematic effects that arise from stochastic nature of biological cells, the imaging apparatus, and optical physics. Such systematic effects are always present in all bioimaging systems and hinder quantitative comparison between the cell model and bioimages. Computational tools for such a comparison are still unavailable. Thus, in this work, we present a computational framework for handling the parameters of the cell models and the optical physics governing bioimaging systems. Simulation using this framework can generate digital images of cell simulation results after accounting for the systematic effects. We then demonstrate that such a framework enables comparison at the level of photon-counting units.

Indexed as

Computer SimulationModels, BiologicalModels, TheoreticalMicroscopy, FluorescencePhotons

Identifiers

PMID26147508
PMCPMC4509736

What OpenQuestion holds

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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.