Evidence map›Paper›PMID 22347386›Full record

ArticlePloS one2012

Segmentation of multi-isotope imaging mass spectrometry data for semi-automatic detection of regions of interest.

Philipp Gormanns, Stefan Reckow, J Collin Poczatek, Christoph W Turck, Claude Lechene

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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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

5 authors.

Philipp GormannsMax Planck Institute of Psychiatry, Proteomics and Biomarkers, Munich, Germany.
Stefan Reckow
J Collin Poczatek
Christoph W Turck
Claude Lechene

Funding

National Resources for Imaging Mass SpectrometryP41EB001974 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI LECHENE, CLAUDE P · 2004 to 2014
$11.8M
Cell fate and tissue turnover in the aged studied with multi-isotope imaging massR21AG034641 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LECHENE, CLAUDE P · 2009 to 2010
$489k
NCRR NIH HHS 2P41 RR0112553-12NIA NIH HHS 1R21AG034641-01NIA NIH HHS R21 AG034641NIA NIH HHS RF-AG-11-001NIBIB NIH HHS 5P41 EB001974-10NIBIB NIH HHS P41 EB001974
6 · The paper itself

Abstract

Multi-isotope imaging mass spectrometry (MIMS) associates secondary ion mass spectrometry (SIMS) with detection of several atomic masses, the use of stable isotopes as labels, and affiliated quantitative image-analysis software. By associating image and measure, MIMS allows one to obtain quantitative information about biological processes in sub-cellular domains. MIMS can be applied to a wide range of biomedical problems, in particular metabolism and cell fate [1], [2], [3]. In order to obtain morphologically pertinent data from MIMS images, we have to define regions of interest (ROIs). ROIs are drawn by hand, a tedious and time-consuming process. We have developed and successfully applied a support vector machine (SVM) for segmentation of MIMS images that allows fast, semi-automatic boundary detection of regions of interests. Using the SVM, high-quality ROIs (as compared to an expert's manual delineation) were obtained for 2 types of images derived from unrelated data sets. This automation simplifies, accelerates and improves the post-processing analysis of MIMS images. This approach has been integrated into "Open MIMS," an ImageJ-plugin for comprehensive analysis of MIMS images that is available online at http://www.nrims.hms.harvard.edu/NRIMS_ImageJ.php.

Indexed as

Support Vector MachineDiagnostic ImagingIsotopesMass SpectrometryMethodsSoftwareIsotopes

Identifiers

PMID22347386
PMCPMC3276494

What OpenQuestion holds

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LicenceCC BY
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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.