Evidence map›Paper›PMID 36978784›Full record

ArticleBioengineering (Basel, Switzerland)2023

GSN-HVNET: A Lightweight, Multi-Task Deep Learning Framework for Nuclei Segmentation and Classification.

Tengfei Zhao, Chong Fu, Yunjia Tian, Wei Song, Chiu-Wing Sham

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Article in Bioengineering (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 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.

Tengfei ZhaoSchool of Computer Science and Engineering, Northeastern University, Shenyang 110819, China.ORCID 0000-0002-0692-0815
Chong FuSchool of Computer Science and Engineering, Northeastern University, Shenyang 110819, China.ORCID 0000-0002-4549-744X
Yunjia TianState Grid Liaoning Information and Communication Company, Shenyang 110006, China.
Wei SongSchool of Computer Science and Engineering, Northeastern University, Shenyang 110819, China.
Chiu-Wing ShamSchool of Computer Science, The University of Auckland, Auckland 1142, New Zealand.

Funding

Fundamental Research Funds for the Central Universities N2116020Fundamental Research Funds for the Central Universities N2224001-7National Natural Science Foundation of China 62032013Natural Science Foundation of Liaoning Province 2021-YGJC-24
6 · The paper itself

Abstract

Nuclei segmentation and classification are two basic and essential tasks in computer-aided diagnosis of digital pathology images, and those deep-learning-based methods have achieved significant success. Unfortunately, most of the existing studies accomplish the two tasks by splicing two related neural networks directly, resulting in repetitive computation efforts and a redundant-and-large neural network. Thus, this paper proposes a lightweight deep learning framework (GSN-HVNET) with an encoder-decoder structure for simultaneous segmentation and classification of nuclei. The decoder consists of three branches outputting the semantic segmentation of nuclei, the horizontal and vertical (HV) distances of nuclei pixels to their mass centers, and the class of each nucleus, respectively. The instance segmentation results are obtained by combing the outputs of the first and second branches. To reduce the computational cost and improve the network stability under small batch sizes, we propose two newly designed blocks, Residual-Ghost-SN (RGS) and Dense-Ghost-SN (DGS). Furthermore, considering the practical usage in pathological diagnosis, we redefine the classification principle of the CoNSeP dataset. Experimental results demonstrate that the proposed model outperforms other state-of-the-art models in terms of segmentation and classification accuracy by a significant margin while maintaining high computational efficiency.

Indexed as

Dense-Ghost-SNjoint nuclei segmentation and classificationlightweight, multi-task deep learning frameworkResidual-Ghost-SN

Identifiers

PMID36978784
PMCPMC10045412

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