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Sheng-Chuan Huang

dblp:310/1255 · DBLP profile ↗
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2ranked-venue papers
0as first author
2since 2021 · last 2023
0000-0003-2860-5119ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Medical and health informatics · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Medical and health informatics › computational pathology
cell detection and classification
0.712023
CW-NET for multitype cell detection and classification in bone marrow examination and mitotic figure examination · Bioinform. 2023
Medical and health informatics
computational pathology
0.712023
CW-NET for multitype cell detection and classification in bone marrow examination and mitotic figure examination · Bioinform. 2023

Methods — techniques the papers use, named apart from their topics

weakly supervised learning · 0.7deep learning · 0.7
YearPublicationVenuePosition
2023 CW-NET for multitype cell detection and classification in bone marrow examination and mitotic figure examination
abstract
MOTIVATION: Bone marrow (BM) examination is one of the most important indicators in diagnosing hematologic disorders and is typically performed under the microscope via oil-immersion objective lens with a total 100× objective magnification. On the other hand, mitotic detection and identification is critical not only for accurate cancer diagnosis and grading but also for predicting therapy success and survival. Fully automated BM examination and mitotic figure examination from whole-slide images is highly demanded but challenging and poorly explored. First, the complexity and poor reproducibility of microscopic image examination are due to the cell type diversity, delicate intralineage discrepancy within the multitype cell maturation process, cells overlapping, lipid interference and stain variation. Second, manual annotation on whole-slide images is tedious, laborious and subject to intraobserver variability, which causes the supervised information restricted to limited, easily identifiable and scattered cells annotated by humans. Third, when the training data are sparsely labeled, many unlabeled objects of interest are wrongly defined as background, which severely confuses AI learners. RESULTS: This article presents an efficient and fully automatic CW-Net approach to address the three issues mentioned above and demonstrates its superior performance on both BM examination and mitotic figure examination. The experimental results demonstrate the robustness and generalizability of the proposed CW-Net on a large BM WSI dataset with 16 456 annotated cells of 19 BM cell types and a large-scale WSI dataset for mitotic figure assessment with 262 481 annotated cells of five cell types. AVAILABILITY AND IMPLEMENTATION: An online web-based system of the proposed method has been created for demonstration (see https://youtu.be/MRMR25Mls1A).
Ching-Wei Wang, Sheng-Chuan Huang, Muhammad Adil Khalil, Ding-Zhi Hong, Shwu-Ing Meng, Yu-Ching Lee
Bioinform.2
2022 Deep learning for bone marrow cell detection and classification on whole-slide images
Ching-Wei Wang, Sheng-Chuan Huang, Yu-Ching Lee, Yu-Jie Shen, Shwu-Ing Meng, Jeff L. Gaol
Medical Image Anal.2