Fei Li

Dr. Fei Li


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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31 March 2017 in BMC Bioinformatics
Verified
Journal Article
Open access
PDF file
Fei LiFei Li
Fei Li
MZMeishan Zhang
Meishan Zhang
GFGuohong Fu
Guohong Fu
DJDonghong Ji
Donghong Ji
Extracting biomedical entities and their relations from text has important applications on biomedical research. Previous work primarily utilized feature-based pipeline models to process this task. Many efforts need to be made on feature engineering when feature-based models are employed. Moreover, pipeline models may suffer error propagation and are not able to utilize the interactions between subtasks. Therefore, we propose a neural joint model to extract biomedical entities as well as their relations simultaneously, and it can alleviate the problems above. Our model was evaluated on two tasks, i.e., the task of extracting adverse drug events between drug and disease entities, and the task of extracting resident relations between bacteria and location entities. Compared with the state-of-the-art systems in these tasks, our model improved the F1 scores of the first task by 5.1% in entity recognition and 8.0% in relation extraction, and that of the second task by 9.2% in relation extraction. The proposed model achieves competitive performances with less work on feature engineering. We demonstrate that the model based on neural networks is effective for biomedical entity and relation extraction. In addition, parameter sharing is an alternative method for neural models to jointly process this task. Our work can facilitate the research on biomedical text mining.

12 September 2019 in JMIR Medical Informatics
Verified
Journal Article
Open access
Fei LiFei Li
Fei Li
YJYonghao Jin
Yonghao Jin
WLWeisong Liu
Weisong Liu
BRBhanu Pratap Singh Rawat
Bhanu Pratap Singh Rawat
PCPengshan Cai
Pengshan Cai
HYHong Yu
Hong Yu
Background: The bidirectional encoder representations from transformers (BERT) model has achieved great success in many natural language processing (NLP) tasks, such as named entity recognition and question answering. However, little prior work has explored this model to be used for an important task in the biomedical and clinical domains, namely entity normalization. Objective: We aim to investigate the effectiveness of BERT-based models for biomedical or clinical entity normalization. In addition, our second objective is to investigate whether the domains of training data influence the performances of BERT-based models as well as the degree of influence. Methods: Our data was comprised of 1.5 million unlabeled electronic health record (EHR) notes. We first fine-tuned BioBERT on this large collection of unlabeled EHR notes. This generated our BERT-based model trained using 1.5 million electronic health record notes (EhrBERT). We then further fine-tuned EhrBERT, BioBERT, and BERT on three annotated corpora for biomedical and clinical entity normalization: the Medication, Indication, and Adverse Drug Events (MADE) 1.0 corpus, the National Center for Biotechnology Information (NCBI) disease corpus, and the Chemical-Disease Relations (CDR) corpus. We compared our models with two state-of-the-art normalization systems, namely MetaMap and disease name normalization (DNorm). Results: EhrBERT achieved 40.95% F1 in the MADE 1.0 corpus for mapping named entities to the Medical Dictionary for Regulatory Activities and the Systematized Nomenclature of Medicine—Clinical Terms (SNOMED-CT), which have about 380,000 terms. In this corpus, EhrBERT outperformed MetaMap by 2.36% in F1. For the NCBI disease corpus and CDR corpus, EhrBERT also outperformed DNorm by improving the F1 scores from 88.37% and 89.92% to 90.35% and 93.82%, respectively. Compared with BioBERT and BERT, EhrBERT outperformed them on the MADE 1.0 corpus and the CDR corpus. Conclusions: Our work shows that BERT-based models have achieved state-of-the-art performance for biomedical and clinical entity normalization. BERT-based models can be readily fine-tuned to normalize any kind of named entities.

1 January 2023
Verified
Conference Paper
Open access
PDF file
FHFei Hao
Fei Hao
BLBobo Li
Bobo Li
QLQian Liu
Qian Liu
LBLidong Bing
Lidong Bing
Fei LiFei Li
Fei Li
TCTat-Seng Chua
Tat-Seng Chua
Hao Fei, Bobo Li, Qian Liu, Lidong Bing, Fei Li, Tat-Seng Chua. Proceedings of the 61st Annual Meeting of the Association for Computational Linguistics (Volume 2: Short Papers). 2023.

26 November 2018 in JMIR Medical Informatics
Verified
Journal Article
Open access
Fei LiFei Li
Fei Li
WLWeisong Liu
Weisong Liu
HYHong Yu
Hong Yu
Journal of Medical Internet Research - International Scientific Journal for Medical Research, Information and Communication on the Internet #Preprint #PeerReviewMe: Warning: This is a unreviewed preprint. Readers are warned that the document has not been peer-reviewed by expert/patient reviewers or an academic editor, may contain misleading claims, and is likely to undergo changes before final publication, if accepted, or may have been rejected/withdrawn. Readers with interest and expertise are encouraged to sign up as peer-reviewer, if the paper is within an open peer-review period. Please cite this preprint only for review purposes or for grant applications and CVs (if you are the author). Background: Adverse drug events (ADEs) are crucial for pharmacovigilance and drug safety surveillance, but main ADE reporting systems such as FAERS face challenges such as underreporting. Therefore, it becomes an important complement to extract ADEs from electronic health record (EHR) notes via natural language processing (NLP). As NLP develops, many up-to-date machine learning techniques are introduced into this area, e.g., deep learning and multi-task learning (MTL). However, few studies focus on employing such techniques to extract ADEs. Objective: We aim to design a deep learning model for extracting ADEs and their related information such as medications and indications. Moreover, since ADE-related information extraction includes two steps, i.e., named entity recognition (NER) and relation extraction (RE), our second objective is to further improve the deep learning model using multi-task learning between the two steps. Methods: We employed the dataset from the MADE1.0 challenge to train and test our models. This dataset consists of 1,089 EHR notes of cancer patients. It includes 9 entity types such as Medication, Indication and ADE, and 7 relation types between these entity types. To extract information from the dataset, we proposed a deep learning model that uses a bi-directional (Bi) long-short-term-memory (LSTM) conditional random field (CRF) network to recognize entities and a BiLSTM-Attention network to extract relations. To further improve the deep learning model, we employed three typical MTL methods, namely hard parameter sharing, parameter regularization and task relation learning, to build three MTL models called HardMTL, RegMTL and LearnMTL respectively. Results: Since ADE-related information extraction is a two-step task, the result of the second step (i.e., relation extraction) is used to compare all the models. We used micro-averaged precision, recall and F1 as evaluation metrics. Our deep learning model achieved the state-of-the-art result (F1=65.9%), which is significantly higher than the result (F1=61.7%) of the best system in the MADE1.0 challenge. HardMTL further improved the F1 by 0.8%, boosting the F1 score to 66.7%, while either RegMTL or LearnMTL failed to boost the performance. Conclusions: Deep learning models are able to significantly improve the performance of ADE-related information extraction. MTL may be effective for NER and RE, but it depends on methods, data and other factors. Our work can facilitate the research on ADE detection, NLP and machine learning.

26 October 2023
Verified
Conference Paper
Open access
BLBobo Li
Bobo Li
FHFei Hao
Fei Hao
LLLizi Liao
Lizi Liao
YZYu Zhao
Yu Zhao
CTChong Teng
Chong Teng
Fei LiFei Li
Fei Li
It has been a hot research topic to enable machines to understand human emotions in multimodal contexts under dialogue scenarios, which is tasked with multimodal emotion analysis in conversation (MM-ERC). MM-ERC has received consistent attention in recent years, where a diverse range of methods has been proposed for securing better task performance. Most existing works treat MM-ERC as a standard multimodal classification problem and perform multimodal feature disentanglement and fusion for maximizing feature utility. Yet after revisiting the characteristic of MM-ERC, we argue that both the feature multimodality and conversational contextualization should be properly modeled simultaneously during the feature disentanglement and fusion steps. In this work, we target further pushing the task performance by taking full consideration of the above insights. On the one hand, during feature disentanglement, based on the contrastive learning technique, we devise a Dual-level Disentanglement Mechanism (DDM) to decouple the features into both the modality space and utterance space. On the other hand, during the feature fusion stage, we propose a Contribution-aware Fusion Mechanism (CFM) and a Context Refusion Mechanism (CRM) for multimodal and context integration, respectively. They together schedule the proper integrations of multimodal and context features. Specifically, CFM explicitly manages the multimodal feature contributions dynamically, while CRM flexibly coordinates the introduction of dialogue contexts. On two public MM-ERC datasets, our system achieves new state-of-the-art performance consistently. Further analyses demonstrate that all our proposed mechanisms greatly facilitate the MM-ERC task by making full use of the multimodal and context features adaptively. Note that our proposed methods have the great potential to facilitate a broader range of other conversational multimodal tasks.

10 May 2022 in Information Processing & Management
Verified
Journal Article
Closed access
CXChunli Xiang
Chunli Xiang
JZJunchi Zhang
Junchi Zhang
Fei LiFei Li
Fei Li
HFHao Fei
Hao Fei
DJDonghong Ji
Donghong Ji