Evidence map›Paper›PMID 28644811›Full record

ArticleIEEE transactions on nanobioscience2017

Applying Pattern Recognition to High-Resolution Images to Determine Cellular Signaling Status.

Michael F Lohrer, Darrin M Hanna, Yang Liu, Kang-Hsin Wang, Fu-Tong Liu, Ted A Laurence, Gang-Yu Liu

Open access · greenAbstract read
In one paragraph

Article in IEEE transactions on nanobioscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.9field-weighted citation impact, top 17% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 3 institutions in 1 country.

Michael F Lohrer
Darrin M Hanna
Yang Liu
Kang-Hsin Wang
Fu-Tong Liu
Ted A Laurence
Gang-Yu Liu
Oakland University · USUniversity of California, Davis · USLawrence Livermore National Laboratory · US

Funding

Nanostructures For Engineering Immune Responses of Dendritic CellsR21CA176850 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LIU, GANG-YU · 2013 to 2014
$331k
NCI NIH HHS R21 CA176850
6 · The paper itself

Abstract

Two frequently used tools to acquire high- resolution images of cells are scanning electron microscopy (SEM) and atomic force microscopy (AFM). The former provides a nanometer resolution view of cellular features rapidly and with high throughput, while the latter enables visualizing hydrated and living cells. In current practice, these images are viewed by eye to determine cellular status, e.g., activated versus resting. Automatic and quantitative data analysis is lacking. This paper develops an algorithm of pattern recognition that works very effectively for AFM and SEM images. Using rat basophilic leukemia cells, our approach creates a support vector machine to automatically classify resting and activated cells. Ten-fold cross-validation with cells that are known to be activated or resting gives a good estimate of the generalized classification results. The pattern recognition of AFM images achieves 100% accuracy, while SEM reaches 95.4% for our images as well as images published in prior literature. This outcome suggests that our methodology could become an important and frequently used tool for researchers utilizing AFM and SEM for structural characterization as well as determining cellular signaling status and function.

Indexed as

AlgorithmsAnimalsCell CommunicationCells, CulturedCell TrackingImage EnhancementLeukemia, Basophilic, AcuteMicroscopy, Atomic ForceMicroscopy, Electron, ScanningMolecular ImagingPattern Recognition, AutomatedRatsReproducibility of ResultsSensitivity and SpecificityTumor Cells, Cultured

Identifiers

PMID28644811
PMCPMC5633003
OpenAlexW2664201349

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.