Fluorescence microscopy and histopathology image based cancer classification using graph convolutional network with channel splitting

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18450%2F25%3A50022120" target="_blank" >RIV/62690094:18450/25:50022120 - isvavai.cz</a>

Alternative codes found

RIV/29142890:_____/25:00052477

Result on the web

<a href="https://www.sciencedirect.com/science/article/pii/S1746809424014587?pes=vor&utm_source=scopus&getft_integrator=scopus" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1746809424014587?pes=vor&utm_source=scopus&getft_integrator=scopus</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.bspc.2024.107400" target="_blank" >10.1016/j.bspc.2024.107400</a>

Result language

angličtina

Original language name

Fluorescence microscopy and histopathology image based cancer classification using graph convolutional network with channel splitting

Original language description

Since the proliferation of deep learning, several convolutional neural networks (CNNs) are developed to attain significant breakthroughs for automated cancer classification using histopathology and fluorescence microscopy images. This work enhances the classification performances of human breast and lung-colon cancers further by exploring a two-layer graph convolutional network (GCN) upon a proposed lightweight deep convolutional backbone or existing pre-trained CNN. The first graph convolution layer considers local regions as the graph nodes with channel information as node features. The second layer is rendered by pooling and splitting the output feature map of former layer into a low dimensional feature vector that serves as node features. The proposed method, named Channel-Splitting Graph Convolutional Network (CS-GCN), enhances holistic feature representation of spatial structural information. The significance of region-aware distinctness is explored for building a correlation among neighboring regions through node-level mixed feature propagation of a graph. The experiments are carried out on three public datasets, representing the breast cancer (actin-labeled fluorescence microscopy image dataset (FMID), and BreakHis dataset with four magnifications), and lung-colon cancer (LC25000 dataset). The top-1 classification accuracies attained by CS-GCN using ResNet-50 backbone on the FMID: 99.30%, BreakHis 40x: 98.0%, BreakHis 100x: 97.81%, BreakHis 200x: 97.33%, BreakHis 400x: 96.85%, and LC25000: 100.0%. The performances are improved on these datasets, while built upon a proposed convolutional stem as well as pre-trained ResNet-50 and DenseNet-201 backbones, implying the effectiveness of the proposed CS-GCN. The source codes are available at: https://github.com/asish-bera/CS-GCN. © 2025 Elsevier Ltd

Czech name

—

Czech description

—

Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

—

OECD FORD branch

10201 - Computer sciences, information science, bioinformathics (hardware development to be 2.2, social aspect to be 5.8)

Project

—

Continuities

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2025

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Biomedical Signal Processing and Control

ISSN

1746-8094

e-ISSN

1746-8108

Volume of the periodical

103

Issue of the periodical within the volume

May

Country of publishing house

GB - UNITED KINGDOM

Number of pages

14

Pages from-to

"Article number: 107400"

UT code for WoS article

001407779500001

EID of the result in the Scopus database

2-s2.0-85213988010