Evidence map›Paper›PMID 24525752›Full record

ArticleNature protocols2014

Segmentation and quantification of subcellular structures in fluorescence microscopy images using Squassh.

Aurélien Rizk, Grégory Paul, Pietro Incardona, Milica Bugarski, Maysam Mansouri, Axel Niemann, Urs Ziegler, Philipp Berger, Ivo F Sbalzarini

Abstract read
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In one paragraph

Article in Nature protocols, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing 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

120 citing papers in PubMed.

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  15. IST1 regulates select recycling pathways.Traffic (Copenhagen, Denmark) · 2024
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  20. Article

60 more citing papers are in PubMed but not listed here.

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.

Aurélien Rizk1] Paul Scherrer Institute, Biomolecular Research, Molecular Cell Biology, Villigen PSI, Switzerland. [2] MOSAIC Group, Center of Systems Biology Dresden, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Grégory Paul1] MOSAIC Group, Center of Systems Biology Dresden, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany. [2].
Pietro IncardonaMOSAIC Group, Center of Systems Biology Dresden, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Milica BugarskiPaul Scherrer Institute, Biomolecular Research, Molecular Cell Biology, Villigen PSI, Switzerland.
Maysam MansouriPaul Scherrer Institute, Biomolecular Research, Molecular Cell Biology, Villigen PSI, Switzerland.
Axel NiemannETH Zurich, Institute of Molecular Health Sciences, Zürich, Switzerland.ORCID 0000000229300950
Urs ZieglerCenter for Microscopy and Image Analysis, University of Zurich, Zürich, Switzerland.
Philipp BergerPaul Scherrer Institute, Biomolecular Research, Molecular Cell Biology, Villigen PSI, Switzerland.
Ivo F SbalzariniMOSAIC Group, Center of Systems Biology Dresden, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detection and quantification of fluorescently labeled molecules in subcellular compartments is a key step in the analysis of many cell biological processes. Pixel-wise colocalization analyses, however, are not always suitable, because they do not provide object-specific information, and they are vulnerable to noise and background fluorescence. Here we present a versatile protocol for a method named 'Squassh' (segmentation and quantification of subcellular shapes), which is used for detecting, delineating and quantifying subcellular structures in fluorescence microscopy images. The workflow is implemented in freely available, user-friendly software. It works on both 2D and 3D images, accounts for the microscope optics and for uneven image background, computes cell masks and provides subpixel accuracy. The Squassh software enables both colocalization and shape analyses. The protocol can be applied in batch, on desktop computers or computer clusters, and it usually requires <1 min and <5 min for 2D and 3D images, respectively. Basic computer-user skills and some experience with fluorescence microscopy are recommended to successfully use the protocol.

Indexed as

SoftwareImage Processing, Computer-AssistedMicroscopy, FluorescenceSubcellular Fractions

Identifiers

PMID24525752

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.