Evidence map›Paper›PMID 21472848›Full record

ArticleCytometry. Part A : the journal of the International Society for Analytical Cytology2011

Image-derived, three-dimensional generative models of cellular organization.

Tao Peng, Robert F Murphy

Open access · bronzeAbstract read
In one paragraph

Article in Cytometry. Part A : the journal of the International Society for Analytical Cytology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 59 citations in OpenAlex.

  1. Learning Morphological, Spatial, and Dynamic Models of Cellular Components.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  2. Article
  3. Article
  4. Article
  5. Data science in cell imaging.Journal of cell science · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Point process models for localization and interdependence of punctate cellular structures.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2016
    Article
  14. Review
  15. Article
  16. Article
  17. Joint modeling of cell and nuclear shape variation.Molecular biology of the cell · 2015
    Article
  18. Article
  19. Extracting meaning from biological imaging data.Molecular biology of the cell · 2014
    Article
  20. Toward the virtual cell: automated approaches to building models of subcellular organization "learned" from microscopy images.BioEssays : news and reviews in molecular, cellular and developmental biology · 2012
    Review
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

2 authors at 2 institutions in 2 countries.

Tao PengCenter for Bioimage Informatics, and Department of Biomedical Engineering, Carnegie Mellon University, 5000 Forbes Ave, Pittsburgh, Pennsylvania 15213, USA.
Robert F Murphy
Carnegie Mellon University · USUniversity of Freiburg · DE

Funding

BUILDING AND VALIDATING LOCATION PROTEOMICS DATABASESR01GM075205 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI MURPHY, ROBERT F · 2007 to 2011
$1.8M
NIGMS NIH HHS R01 GM 075205NIGMS NIH HHS R01 GM075205
6 · The paper itself

Abstract

Given the importance of subcellular location to protein function, computational simulations of cell behaviors will ultimately require the ability to model the distributions of proteins within organelles and other structures. Toward this end, statistical learning methods have previously been used to build models of sets of two-dimensional microscope images, where each set contains multiple images for a single subcellular location pattern. The model learned from each set of images not only represents the pattern but also captures the variation in that pattern from cell to cell. The models consist of sub-models for nuclear shape, cell shape, organelle size and shape, and organelle distribution relative to nuclear and cell boundaries, and allow synthesis of images with the expectation that they are drawn from the same underlying statistical distribution as the images used to train them. Here we extend this generative models approach to three dimensions using a similar framework, permitting protein subcellular locations to be described more accurately. Models of different patterns can be combined to yield a synthetic multi-channel image containing as many proteins as desired, something that is difficult to obtain by direct microscope imaging for more than a few proteins. In addition, the model parameters represent a more compact and interpretable way of communicating subcellular patterns than descriptive image features and may be particularly effective for automated identification of changes in subcellular organization caused by perturbagens.

Indexed as

Models, BiologicalPattern Recognition, AutomatedCellular StructuresHeLa CellsHumansImaging, Three-DimensionalProteinsProteins

Identifiers

PMID21472848
PMCPMC3127045
OpenAlexW2125493690

What OpenQuestion holds

Textmetadata
LicenceTDM
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.