Xiaolong Wang

Prof. Xiaolong Wang

the College of Computer Science and Technology, Harbin Institute of Technology, Shenzhen
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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5 July 2017 in BMC Medical Informatics and Decision Making
Verified
Journal Article
Open access
PDF file
ZLZengjian Liu
Zengjian Liu
MYMing Yang
Ming Yang
XWXiaolong Wang
Xiaolong Wang
QCQingcai Chen
Qingcai Chen
BTBuzhou Tang
Buzhou Tang
HXHua Xu
Hua Xu
Entity recognition is one of the most primary steps for text analysis and has long attracted considerable attention from researchers. In the clinical domain, various types of entities, such as clinical entities and protected health information (PHI), widely exist in clinical texts. Recognizing these entities has become a hot topic in clinical natural language processing (NLP), and a large number of traditional machine learning methods, such as support vector machine and conditional random field, have been deployed to recognize entities from clinical texts in the past few years. In recent years, recurrent neural network (RNN), one of deep learning methods that has shown great potential on many problems including named entity recognition, also has been gradually used for entity recognition from clinical texts. In this paper, we comprehensively investigate the performance of LSTM (long-short term memory), a representative variant of RNN, on clinical entity recognition and protected health information recognition. The LSTM model consists of three layers: input layer – generates representation of each word of a sentence; LSTM layer – outputs another word representation sequence that captures the context information of each word in this sentence; Inference layer – makes tagging decisions according to the output of LSTM layer, that is, outputting a label sequence. Experiments conducted on corpora of the 2010, 2012 and 2014 i2b2 NLP challenges show that LSTM achieves highest micro-average F1-scores of 85.81% on the 2010 i2b2 medical concept extraction, 92.29% on the 2012 i2b2 clinical event detection, and 94.37% on the 2014 i2b2 de-identification, which is considerably competitive with other state-of-the-art systems. LSTM that requires no hand-crafted feature has great potential on entity recognition from clinical texts. It outperforms traditional machine learning methods that suffer from fussy feature engineering. A possible future direction is how to integrate knowledge bases widely existing in the clinical domain into LSTM, which is a case of our future work. Moreover, how to use LSTM to recognize entities in specific formats is also another possible future direction.

1 November 2017 in Journal of Biomedical Informatics
Verified
Journal Article
Closed access
ZLZengjian Liu
Zengjian Liu
BTBuzhou Tang
Buzhou Tang
XWXiaolong Wang
Xiaolong Wang
QCQingcai Chen
Qingcai Chen

9 October 2017 in Briefings in Bioinformatics
Verified
Journal Article
Closed access
PDF file
YLYumeng Liu
Yumeng Liu
XWXiaolong Wang
Xiaolong Wang
BLBin Liu
Bin Liu
Intrinsically disordered proteins and regions are widely distributed in proteins, which are associated with many biological processes and diseases. Accurate prediction of intrinsically disordered proteins and regions is critical for both basic research (such as protein structure and function prediction) and practical applications (such as drug development). During the past decades, many computational approaches have been proposed, which have greatly facilitated the development of this important field. Therefore, a comprehensive and updated review is highly required. In this regard, we give a review on the computational methods for intrinsically disordered protein and region prediction, especially focusing on the recent development in this field. These computational approaches are divided into four categories based on their methodologies, including physicochemical-based method, machine-learning-based method, template-based method and meta method. Furthermore, their advantages and disadvantages are also discussed. The performance of 40 state-of-the-art predictors is directly compared on the target proteins in the task of disordered region prediction in the 10th Critical Assessment of protein Structure Prediction. A more comprehensive performance comparison of 45 different predictors is conducted based on seven widely used benchmark data sets. Finally, some open problems and perspectives are discussed.

13 November 2016 in Briefings in Bioinformatics
Verified
Journal Article
Open access
PDF file
JCJunjie Chen
Junjie Chen
MGMingyue Guo
Mingyue Guo
XWXiaolong Wang
Xiaolong Wang
BLBin Liu
Bin Liu
Protein remote homology detection is one of the most fundamental and central problems for the studies of protein structures and functions, aiming to detect the distantly evolutionary relationships among proteins via computational methods. During the past decades, many computational approaches have been proposed to solve this important task. These methods have made a substantial contribution to protein remote homology detection. Therefore, it is necessary to give a comprehensive review and comparison on these computational methods. In this article, we divide these computational approaches into three categories, including alignment methods, discriminative methods and ranking methods. Their advantages and disadvantages are discussed in a comprehensive perspective, and their performance is compared on widely used benchmark data sets. Finally, some open questions in this field are further explored and discussed.

18 June 2015 in Molecular Genetics and Genomics
Verified
Journal Article
Closed access
PDF file
BLBin Liu
Bin Liu
FLFule Liu
Fule Liu
LFLongyun Fang
Longyun Fang
XWXiaolong Wang
Xiaolong Wang
KCKuo-Chen Chou
Kuo-Chen Chou

1 November 2015 in Journal of Theoretical Biology
Verified
Journal Article
Closed access
BLBin Liu
Bin Liu
LFLongyun Fang
Longyun Fang
SWShanyi Wang
Shanyi Wang
XWXiaolong Wang
Xiaolong Wang
HLHongtao Li
Hongtao Li
KCKuo-Chen Chou
Kuo-Chen Chou