Evidence map›Paper›PMID 36479023›Full record

ArticleComputational intelligence and neuroscience2022

Cell Phenotype Classification Based on Joint of Texture Information and Multilayer Feature Extraction in DenseNet.

Shervan Fekri-Ershad, Mustafa Jawad Al-Imari, Mohammed Hayder Hamad, Marwa Fadhil Alsaffar, Fuad Ghazi Hassan, Mazin Eidan Hadi, Karrar Salih Mahdi

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Article in Computational intelligence and neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

7 authors.

Shervan Fekri-ErshadFaculty of Computer Engineering, Najafabad Branch, Islamic Azad University, Najafabad, Iran.ORCID https://orcid.org/0000-0003-1226-7610
Mustafa Jawad Al-ImariDepartment of Medical Laboratory Techniques, Al-Mustaqbal University College, Hillah 51001, Babylon, Iraq.ORCID https://orcid.org/0000-0002-7313-7580
Mohammed Hayder HamadDepartment of Medical Laboratory Techniques, Al-Mustaqbal University College, Hillah 51001, Babylon, Iraq.
Marwa Fadhil AlsaffarDepartment of Medical Laboratory Techniques, Al-Mustaqbal University College, Hillah 51001, Babylon, Iraq.
Fuad Ghazi HassanDepartment of Medical Laboratory Techniques, Al-Mustaqbal University College, Hillah 51001, Babylon, Iraq.
Mazin Eidan HadiDepartment of Medical Laboratory Techniques, Al-Mustaqbal University College, Hillah 51001, Babylon, Iraq.ORCID https://orcid.org/0000-0002-4157-9106
Karrar Salih MahdiDepartment of Medical Laboratory Techniques, Al-Mustaqbal University College, Hillah 51001, Babylon, Iraq.ORCID https://orcid.org/0000-0002-4717-6156

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell phenotype classification is a critical task in many medical applications, such as protein localization, gene effect identification, and cancer diagnosis in some types. Fluorescence imaging is the most efficient tool to analyze the biological characteristics of cells. So cell phenotype classification in fluorescence microscopy images has received increased attention from scientists in the last decade. The visible structures of cells are usually different in terms of shape, texture, relationship between intensities, etc. In this scope, most of the presented approaches use one type or joint of low-level and high-level features. In this paper, a new approach is proposed based on a combination of low-level and high-level features. An improved version of local quinary patterns is used to extract low-level texture features. Also, an innovative multilayer deep feature extraction method is performed to extract high-level features from DenseNet. In this respect, an output feature map of dense blocks is entered in a separate way to pooling and flatten layers, and finally, feature vectors are concatenated. The performance of the proposed approach is evaluated on the benchmark dataset 2D-HeLa in terms of accuracy. Also, the proposed approach is compared with state-of-the-art methods in terms of classification accuracy. Comparison of results demonstrates higher performance of the proposed approach in comparison with some efficient methods.

Identifiers

PMID36479023
PMCPMC9722294

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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.