Evidence map›Paper›PMID 22482949›Full record

ArticleMethods in cell biology2012

CellOrganizer: Image-derived models of subcellular organization and protein distribution.

Robert F Murphy

Abstract read
In one paragraph

Article in Methods in cell biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cell Membrane Tracking in Living Brain Tissue Using Differential Interference Contrast Microscopy.IEEE transactions on image processing : a publication of the IEEE Signal Processing Society · 2018
    Article
  10. Review
  11. 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
  12. Review
  13. Article
  14. Visualizing quantitative microscopy data: History and challenges.Critical reviews in biochemistry and molecular biology · 2016
    Review
  15. Article
  16. Joint modeling of cell and nuclear shape variation.Molecular biology of the cell · 2015
    Article
  17. Review
  18. 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

1 author.

Robert F MurphyLane Center for Computational Biology, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.

Funding

Image-derived Spatiotemporal Models of Cellular Organization and PerturbationR01GM090033 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI MURPHY, ROBERT F, ROHDE, GUSTAVO KUNDE · 2010 to 2018
$2.4M
BUILDING AND VALIDATING LOCATION PROTEOMICS DATABASESR01GM075205 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI MURPHY, ROBERT F · 2007 to 2011
$1.8M
ROBUST PORTABLE SOFTWARE FOR LOCATION PROTEOMICSR01GM068845 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI MURPHY, ROBERT F. · 2003 to 2006
$806k
NIGMS NIH HHS GM068845NIGMS NIH HHS GM075205NIGMS NIH HHS GM090033NIGMS NIH HHS R01 GM068845NIGMS NIH HHS R01 GM075205NIGMS NIH HHS R01 GM090033
6 · The paper itself

Abstract

This chapter describes approaches for learning models of subcellular organization from images. The primary utility of these models is expected to be from incorporation into complex simulations of cell behaviors. Most current cell simulations do not consider spatial organization of proteins at all, or treat each organelle type as a single, idealized compartment. The ability to build generative models for all proteins in a proteome and use them for spatially accurate simulations is expected to improve the accuracy of models of cell behaviors. A second use, of potentially equal importance, is expected to be in testing and comparing software for analyzing cell images. The complexity and sophistication of algorithms used in cell-image-based screens and assays (variously referred to as high-content screening, high-content analysis, or high-throughput microscopy) is continuously increasing, and generative models can be used to produce images for testing these algorithms in which the expected answer is known.

Indexed as

Models, BiologicalAlgorithmsAnimalsCell CompartmentationCell LineCell ShapeCytoskeletonHumansImage Processing, Computer-AssistedMiceMicroscopy, FluorescenceOrganellesOrganelle ShapeProteinsProtein TransportProteomicsProteins

Identifiers

PMID22482949
PMCPMC4107418

What OpenQuestion holds

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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.