Portrait of Yue Li

Yue Li

Associate Academic Member
Assistant Professor, McGill University, School of Computer Science
Research Topics
AI in Health
Bayesian Models
Computational Biology
Deep Learning
Genetics
Large Language Models (LLM)
Multimodal Learning
Single-Cell Genomics

Biography

I completed my PhD degree in computer science and computational biology at the University of Toronto in 2014. Prior to joining McGill University, I was a postdoctoral associate at the Computer Science and Artificial Intelligence Laboratory (CSAIL) at MIT (2015–2018).

In general, my research program covers three main research areas that involve applied machine learning in computational genomics and health. More specifically, it focuses on developing interpretable probabilistic learning models and deep learning models to model genetic, epigenetic, electronic health record and single-cell genomic data.

By systematically integrating multimodal and longitudinal data, I aim to have impactful applications in computational medicine, including building intelligent clinical recommender systems, forecasting patient health trajectories, making personalized polygenic risk predictions, characterizing multi-trait functional genetic mutations, and dissecting cell-type-specific regulatory elements that underpin complex traits and diseases in humans.

Current Students

Postdoctorate - McGill University
PhD - McGill University
Master's Research - McGill University
Master's Research - McGill University
Master's Research - McGill University
PhD - McGill University
Master's Research - McGill University
Principal supervisor :
PhD - McGill University
Master's Research - McGill University
Co-supervisor :
PhD - McGill University
Master's Research - McGill University
Postdoctorate - McGill University
Co-supervisor :
PhD - McGill University

Publications

TimelyGPT: Extrapolatable Transformer Pre-training for Long-term Time-Series Forecasting in Healthcare
Ziyang Song
Qincheng Lu
Hao Xu
Mike He Zhu
Motivation: Large-scale pre-trained models (PTMs) such as BERT and GPT have recently achieved great success in Natural Language Processing a… (see more)nd Computer Vision domains. However, the development of PTMs on healthcare time-series data is lagging behind. This underscores the limitations of the existing transformer-based architectures, particularly their scalability to handle large-scale time series and ability to capture long-term temporal dependencies. Methods: In this study, we present Timely Generative Pre-trained Transformer (TimelyGPT). TimelyGPT employs an extrapolatable position (xPos) embedding to encode trend and periodic patterns into time-series representations. It also integrates recurrent attention and temporal convolution modules to effectively capture global-local temporal dependencies. Materials: We evaluated TimelyGPT on two large-scale healthcare time series datasets corresponding to continuous biosignals and irregularly-sampled time series, respectively: (1) the Sleep EDF dataset consisting of over 1.2 billion timesteps; (2) the longitudinal healthcare administrative database PopHR, comprising 489,000 patients randomly sampled from the Montreal population. Results: In forecasting continuous biosignals, TimelyGPT achieves accurate extrapolation up to 6,000 timesteps of body temperature during the sleep stage transition, given a short look-up window (i.e., prompt) containing only 2,000 timesteps. For irregularly-sampled time series, TimelyGPT with a proposed time-specific inference demonstrates high top recall scores in predicting future diagnoses using early diagnostic records, effectively handling irregular intervals between clinical records. Together, we envision TimelyGPT to be useful in various health domains, including long-term patient health state forecasting and patient risk trajectory prediction. Availability: The open-sourced code is available at Github.
MDFD: Study of Distributed Non-IID Scenarios and Frechet Distance-Based Evaluation
Wei Wang
Mingwei Zhang
Ziwen Wu
Qianxi Chen
With the development of distributed machine learning and federated learning, the solution to the data island problem is promoted. People use… (see more) computer clusters to train machine learning models on data distributed in different regions. In the early stage of research, researchers usually assume that the data sets of each node are independent identically distribution (IID), but this is a strong assumption, which is challenging to meet in practical applications. Therefore, research on non-IID has become a hot spot in recent years. However, there is no uniform standard for designing and evaluating non-IID scenarios. This paper proposes a Frechet distance-independent non-IID distribution dataset metric MDFD. And we conducted experiments on different types of distributed machine-learning methods in different non-IID scenarios to verify the effectiveness of MDFD.
SDWD: Style Diversity Weighted Distance Evaluates the Intra-Class Data Diversity of Distributed GANs
Wei Wang
Ziwen Wu
Mingwei Zhang
Differential Chromatin Architecture and Risk Variants in Deep Layer Excitatory Neurons and Grey Matter Microglia Contribute to Major Depressive Disorder
Anjali Chawla
Wenmin Zhang
Malosree Maitra
Reza Rahimian
Haruka Mitsuhashi
MA Davoli
Jenny Yang
Gary Gang Chen
Ryan Denniston
Deborah Mash
Naguib Mechawar
Matthew Suderman
Corina Nagy
Gustavo Turecki
GTM-decon: guided-topic modeling of single-cell transcriptomes enables sub-cell-type and disease-subtype deconvolution of bulk transcriptomes
Lakshmipuram Seshadri Swapna
Michael Huang
Guided-topic modelling of single-cell transcriptomes enables sub-cell-type and disease-subtype deconvolution of bulk transcriptomes
Lakshmipuram Seshadri Swapna
Michael Huang
Cell-type composition is an important indicator of health. We present Guided Topic Model for deconvolution (GTM-decon) to automatically infe… (see more)r cell-type-specific gene topic distributions from single-cell RNA-seq data for deconvolving bulk transcriptomes. GTM-decon performs competitively on deconvolving simulated and real bulk data compared with the state-of-the-art methods. Moreover, as demonstrated in deconvolving disease transcriptomes, GTM-decon can infer multiple cell-type-specific gene topic distributions per cell type, which captures sub-cell-type variations. GTM-decon can also use phenotype labels from single-cell or bulk data as a guide to infer phenotype-specific gene distributions. In a nested-guided design, GTM-decon identified cell-type-specific differentially expressed genes from bulk breast cancer transcriptomes.
Biomedical discovery through the integrative biomedical knowledge hub (iBKH).
Chang Su
Yufang Hou
Manqi Zhou
Suraj Rajendran
Jacqueline R.M. A. Maasch
Zehra Abedi
Haotan Zhang
Zilong Bai
Anthony Cuturrufo
Winston Guo
Fayzan F. Chaudhry
Gregory Ghahramani
Feixiong Cheng
Rui Zhang
Steven T. DeKosky
Jiang Bian
Yi Wang
Single-cell multi-omic topic embedding reveals cell-type-specific and COVID-19 severity-related immune signatures
Manqi Zhou
Hao Zhang
Zilong Bai
Yi Wang
The advent of single-cell multi-omics sequencing technology makes it possible for re-searchers to leverage multiple modalities for individua… (see more)l cells and explore cell heterogeneity. However, the high dimensional, discrete, and sparse nature of the data make the downstream analysis particularly challenging. Most of the existing computational methods for single-cell data analysis are either limited to single modality or lack flexibility and interpretability. In this study, we propose an interpretable deep learning method called multi-omic embedded topic model (moETM) to effectively perform integrative analysis of high-dimensional single-cell multimodal data. moETM integrates multiple omics data via a product-of-experts in the encoder for efficient variational inference and then employs multiple linear decoders to learn the multi-omic signatures of the gene regulatory programs. Through comprehensive experiments on public single-cell transcriptome and chromatin accessibility data (i.e., scRNA+scATAC), as well as scRNA and proteomic data (i.e., CITE-seq), moETM demonstrates superior performance compared with six state-of-the-art single-cell data analysis methods on seven publicly available datasets. By applying moETM to the scRNA+scATAC data in human bone marrow mononuclear cells (BMMCs), we identified sequence motifs corresponding to the transcription factors that regulate immune gene signatures. Applying moETM analysis to CITE-seq data from the COVID-19 patients revealed not only known immune cell-type-specific signatures but also composite multi-omic biomarkers of critical conditions due to COVID-19, thus providing insights from both biological and clinical perspectives.
Modeling electronic health record data using an end-to-end knowledge-graph-informed topic model
Yuesong Zou
Ahmad Pesaranghader
Ziyang Song
Aman Verma
MixEHR-Guided: A guided multi-modal topic modeling approach for large-scale automatic phenotyping using the electronic health record
Yuri Ahuja
Yuesong Zou
Aman Verma
Automatic Phenotyping by a Seed-guided Topic Model
Ziyang Song
Yuanyi Hu
Aman Verma
Electronic health records (EHRs) provide rich clinical information and the opportunities to extract epidemiological patterns to understand a… (see more)nd predict patient disease risks with suitable machine learning methods such as topic models. However, existing topic models do not generate identifiable topics each predicting a unique phenotype. One promising direction is to use known phenotype concepts to guide topic inference. We present a seed-guided Bayesian topic model called MixEHR-Seed with 3 contributions: (1) for each phenotype, we infer a dual-form of topic distribution: a seed-topic distribution over a small set of key EHR codes and a regular topic distribution over the entire EHR vocabulary; (2) we model age-dependent disease progression as Markovian dynamic topic priors; (3) we infer seed-guided multi-modal topics over distinct EHR data types. For inference, we developed a variational inference algorithm. Using MixEHR-Seed, we inferred 1569 PheCode-guided phenotype topics from an EHR database in Quebec, Canada covering 1.3 million patients for up to 20-year follow-up with 122 million records for 8539 and 1126 unique diagnostic and drug codes, respectively. We observed (1) accurate phenotype prediction by the guided topics, (2) clinically relevant PheCode-guided disease topics, (3) meaningful age-dependent disease prevalence. Source code is available at GitHub: https://github.com/li-lab-mcgill/MixEHR-Seed.
Modeling electronic health record data using a knowledge-graph-embedded topic model
Yuesong Zou
Ahmad Pesaranghader
Aman Verma
The rapid growth of electronic health record (EHR) datasets opens up promising opportunities to understand human diseases in a systematic wa… (see more)y. However, effective extraction of clinical knowledge from the EHR data has been hindered by its sparsity and noisy information. We present KG-ETM, an end-to-end knowledge graph-based multimodal embedded topic model. KG-ETM distills latent disease topics from EHR data by learning the embedding from the medical knowledge graphs. We applied KG-ETM to a large-scale EHR dataset consisting of over 1 million patients. We evaluated its performance based on EHR reconstruction and drug imputation. KG-ETM demonstrated superior performance over the alternative methods on both tasks. Moreover, our model learned clinically meaningful graph-informed embedding of the EHR codes. In additional, our model is also able to discover interpretable and accurate patient representations for patient stratification and drug recommendations.