Evidence map›Paper›PMID 30687900›Full record

ArticleMedical & biological engineering & computing2019

Fluorescence microscopy image classification of 2D HeLa cells based on the CapsNet neural network.

XiaoQing Zhang, Shu-Guang Zhao

Abstract read
PubMed Publisher
In one paragraph

Article in Medical & biological engineering & computing, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

2 authors.

XiaoQing ZhangCollege of Information Science and Technology, Donghua University, Shanghai, 201620, China. zxq_005@163.com.ORCID http://orcid.org/0000-0002-1072-6652
Shu-Guang ZhaoCollege of Information Science and Technology, Donghua University, Shanghai, 201620, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of computer technology now allows the quick and efficient automatic fluorescence microscopy generation of a large number of images of proteins in specific subcellular compartments using fluorescence microscopy. Digital image processing and pattern recognition technology can easily classify these images, identify the subcellular location of proteins, and subsequently carry out related work such as analysis and investigation of protein function. Here, based on a fluorescence microscopy 2D image dataset of HeLa cells, the CapsNet network model was used to classify ten types of images of proteins in different subcellular compartments. Capsules in the CapsNet network model were trained to capture the possibility of certain features and variants rather than to capture the characteristics of a specific variant. The capsule at the same level predicted the instantiation parameters of the higher level capsule through the transformation matrix, and the higher level capsule became active when multiple dynamic routing forecasts were consistent. Experiments show that using the CapsNet network model to classify 2D HeLa datasets can achieve higher accuracy. Graphical abstract ᅟ.

Indexed as

Neural Networks, ComputerActinsHeLa CellsHumansImage Processing, Computer-AssistedMicroscopy, FluorescenceSupport Vector MachineActins2D HeLaCapsNetFluorescence microscopyImage classificationNeural networkSubcellular localization

Identifiers

What OpenQuestion holds

Textmetadata
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.