Jinwen Ma

Prof. Jinwen Ma

Department of Information Science, School of Mathematical Sciences and LMAM, Peking University, Beijing 100871, China
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2021 in Computerized Medical Imaging and Graphics
Verified
Journal Article
Closed access
Imran IqbalImran Iqbal
Imran Iqbal
MYMUHAMMAD YOUNUS
MUHAMMAD YOUNUS
KWKhuram Walayat
Khuram Walayat
MKMohib Ullah Kakar
Mohib Ullah Kakar
Jinwen MaJinwen Ma
Jinwen Ma

6 October 2018
Verified
Book Chapter
Closed access
PDF file
TXTaihong Xiao
Taihong Xiao
JHJiapeng Hong
Jiapeng Hong
Jinwen MaJinwen Ma
Jinwen Ma

15 July 2020 in IET Image Processing
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Journal Article
Open access
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Imran IqbalImran Iqbal
Imran Iqbal
GSGhazala Shahzad
Ghazala Shahzad
NRNida Rafiq
Nida Rafiq
GMGhulam Mustafa
Ghulam Mustafa
Jinwen MaJinwen Ma
Jinwen Ma
As an analytic tool in medicine, particularly in radiology, deep learning is gaining much attention and opening a new way for disease diagnosis. Nonetheless, it is rather challenging to acquire large‐scale detailed labelled datasets in the field of medical imaging. In fact, transfer learning provides a possible way to resolve this issue to a certain extent such that the parameter learning of a neural network starts with its pre‐trained weights learned from a large‐scale dataset of certain similar task, and fine‐tunes on a small comprehensively annotated dataset for the particular target task. The main aim of this study is to apply the deep learning model to detect the synovial fluid of human knee joint from magnetic resonance images. A specialized convolutional neural network architecture is proposed for automated detection of human knee joint's synovial fluid. Two independent datasets are used in the training, development, and evaluation of the proposed model. It is demonstrated by the experimental results that the proposed model obtains high sensitivity, specificity, precision, and accuracy to the detection of human knee joint's synovial fluid. As a result, this proposed approach provides a novel and feasible way for automating and expediting the synovial fluid analysis.

20 May 2020 in Diagnostics
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Journal Article
Open access
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Imran IqbalImran Iqbal
Imran Iqbal
GMGhulam Mustafa
Ghulam Mustafa
Jinwen MaJinwen Ma
Jinwen Ma
Human infertility is considered as a serious disease of the reproductive system that affects more than 10% of couples across the globe and over 30% of the reported cases are related to men. The crucial step in the assessment of male infertility and subfertility is semen analysis that strongly depends on the sperm head morphology, i.e., the shape and size of the head of a spermatozoon. However, in medical diagnosis, the morphology of the sperm head is determined manually, and heavily depends on the expertise of the clinician. Moreover, this assessment as well as the morphological classification of human sperm heads are laborious and non-repeatable, and there is also a high degree of inter and intra-laboratory variability in the results. In order to overcome these problems, we propose a specialized convolutional neural network (CNN) architecture to accurately classify human sperm heads based on sperm images. It is carefully designed with several layers, and multiple filter sizes, but fewer filters and parameters to improve efficiency and effectiveness. It is demonstrated that our proposed architecture outperforms state-of-the-art methods, exhibiting 88% recall on the SCIAN dataset in the total agreement setting and 95% recall on the HuSHeM dataset for the classification of human sperm heads. Our proposed method shows the potential of deep learning to surpass embryologists in terms of reliability, throughput, and accuracy.

28 July 2009 in IEEE Transactions on Medical Imaging
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Journal Article
Closed access
FLFuhai Li
Fuhai Li
XZXiaobo Zhou
Xiaobo Zhou
Jinwen MaJinwen Ma
Jinwen Ma
SWStephen T. C. Wong
Stephen T. C. Wong
Automated cell segmentation and tracking are critical for quantitative analysis of cell cycle behavior using time-lapse fluorescence microscopy. However, the complex, dynamic cell cycle behavior poses new challenges to the existing image segmentation and tracking methods. This paper presents a fully automated tracking method for quantitative cell cycle analysis. In the proposed tracking method, we introduce a neighboring graph to characterize the spatial distribution of neighboring nuclei, and a novel dissimilarity measure is designed based on the spatial distribution, nuclei morphological appearance, migration, and intensity information. Then, we employ the integer programming and division matching strategy, together with the novel dissimilarity measure, to track cell nuclei. We applied this new tracking method for the tracking of HeLa cancer cells over several cell cycles, and the validation results showed that the high accuracy for segmentation and tracking at 99.5% and 90.0%, respectively. The tracking method has been implemented in the cell-cycle analysis software package, DCELLIQ, which is freely available.

26 October 2017
Verified
Book Chapter
Closed access
PDF file
SLShuanglong Liu
Shuanglong Liu
CZChao Zhang
Chao Zhang
Jinwen MaJinwen Ma
Jinwen Ma