Eugene Lin

ORCID: 0000-0001-6984-2159
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About
Contact & Profiles
Research Areas
  • Genetic Associations and Epidemiology
  • Bioinformatics and Genomic Networks
  • Diet and metabolism studies
  • Tryptophan and brain disorders
  • Gene expression and cancer classification
  • Machine Learning in Healthcare
  • Computational Drug Discovery Methods
  • Hepatitis C virus research
  • Adipose Tissue and Metabolism
  • Epigenetics and DNA Methylation
  • Liver Disease Diagnosis and Treatment
  • Nutrition, Genetics, and Disease
  • Treatment of Major Depression
  • Neurotransmitter Receptor Influence on Behavior
  • Schizophrenia research and treatment
  • Mental Health Research Topics
  • Genetics and Neurodevelopmental Disorders
  • Receptor Mechanisms and Signaling
  • Diabetes Treatment and Management
  • RNA and protein synthesis mechanisms
  • Diet, Metabolism, and Disease
  • Hepatitis B Virus Studies
  • Amino Acid Enzymes and Metabolism
  • Circadian rhythm and melatonin
  • Nerve injury and regeneration

China Medical University
2015-2025

University of Washington
1999-2025

Seattle University
2016-2020

Genomics Research Center, Academia Sinica
2008-2017

Genomics (United Kingdom)
2008-2017

Scientific Fishery Systems (United States)
2016-2017

National Chung Hsing University
2007-2013

Chang Bing Show Chwan Memorial Hospital
2013

Central Taiwan University of Science and Technology
2007

Chaoyang University of Technology
2007

Generative Adversarial networks (GANs) have obtained remarkable success in many unsupervised learning tasks and unarguably, clustering is an important problem. While one can potentially exploit the latent-space back-projection GANs to cluster, we demonstrate that cluster structure not retained GAN latent space. In this paper, propose ClusterGAN as a new mechanism for using GANs. By sampling variables from mixture of one-hot encoded continuous variables, coupled with inverse network (which...

10.1609/aaai.v33i01.33014610 article EN Proceedings of the AAAI Conference on Artificial Intelligence 2019-07-17

In the wake of recent advances in scientific research, personalized medicine using deep learning techniques represents a new paradigm. this work, our goal was to establish models which distinguish responders from non-responders, and also predict possible antidepressant treatment outcomes major depressive disorder (MDD). To uncover relationships between responsiveness biomarkers, we developed prediction approach resulting analysis genetic clinical factors such as single nucleotide...

10.3389/fpsyt.2018.00290 article EN cc-by Frontiers in Psychiatry 2018-07-06

Abstract Background Single-cell RNA sequencing (scRNA-seq) is an emerging technology that can assess the function of individual cell and cell-to-cell variability at single level in unbiased manner. Dimensionality reduction essential first step downstream analysis scRNA-seq data. However, data are challenging for traditional methods due to their high dimensional measurements as well abundance dropout events (that is, zero expression measurements). Results To overcome these difficulties, we...

10.1186/s12859-020-3401-5 article EN cc-by BMC Bioinformatics 2020-02-21

Depression is associated with various environmental risk factors such as stress, childhood maltreatment experiences, and stressful life events. Current approaches to assess the pathophysiology of depression, epigenetics gene-environment (GxE) interactions, have been widely leveraged determine plausible markers, genes, variants for developing depression.We focus on most recent developments genomic research in GxE interactions.In this review, we first survey a variety association studies...

10.30773/pi.2019.07.17.2 article EN Psychiatry Investigation 2019-08-28

Abstract Increased risk of developing metabolic syndrome (MetS) has been associated with the APOA5 , APOC1 BRAP BUD13 CETP LIPA LPL PLCG1 and ZPR1 genes. In this replication study, we reassessed whether these genes are MetS its individual components independently and/or through complex interactions in a Taiwanese population. We also analyzed between environmental factors influencing components. A total 3,000 subjects were assessed study. Metabolic traits such as waist circumference,...

10.1038/srep36830 article EN cc-by Scientific Reports 2016-11-09

In the studies of genomics, it is essential to select a small number genes that are more significant than others for association disease susceptibility. this work, our goal was compare computational tools with and without feature selection predicting chronic fatigue syndrome (CFS) using genetic factors such as single nucleotide polymorphisms (SNPs).We employed dataset original previous study by CDC Chronic Fatigue Syndrome Research Group. To uncover relationships between CFS SNPs, we applied...

10.1186/1479-5876-7-81 article EN cc-by Journal of Translational Medicine 2009-09-22

Brain-derived neurotrophic-factor (BDNF) and its receptor neurotrophic tyrosine kinase 2 (NTRK2) have been implicated in both major depression cognitive function. This study examines the main effects of single loci multilocus interactions to test hypothesis that BDNF NTRK2 genes may contribute etiology geriatric independently and/or through complex interactions. We genotyped gene Val66Met (rs6265) polymorphism four single-nucleotide polymorphisms (SNPs) (including rs1187323, rs1187329,...

10.1089/rej.2009.0871 article EN Rejuvenation Research 2009-12-01

The transforming growth factor-β (TGF-β) signaling pathway and its relevant genes have been correlated with an increased risk of developing various hallmarks metabolic syndrome (MetS). In this study, we assessed whether the TGF-β pathway-associated SMAD family member 2 (SMAD2), SMAD3, SMAD4, factor beta 1 (TGFB1), TGFB2, TGFB3, receptor (TGFBR1), TGFBR2 are associated MetS individual components independently, through complex interactions, or both in a Taiwanese population. A total 3,000...

10.1038/s41598-017-14025-4 article EN cc-by Scientific Reports 2017-10-13

Abstract It has been suggested that the relationship between cognitive function and functional outcome in schizophrenia is mediated by clinical symptoms, while assessed Quality of Life Scale (QLS) Global Assessment Functioning (GAF) Scale. To determine QLS GAF, we established a bagging ensemble framework with feature selection algorithm resulting from analysis factors such as 3 symptom scales 11 scores 302 patients Taiwanese population. We compared our other state-of-the-art algorithms...

10.1038/s41598-021-86382-0 article EN cc-by Scientific Reports 2021-03-25

Machine learning has been proposed to utilize d-amino acid oxidase (DAO) and DAO activator (DAOA [or pLG72]) protein levels ascertain disease status in schizophrenia. However, it remains unclear whether machine can effectively evaluate clinical features relation DAOA schizophrenia patients. We employed an interpretable (IML) framework including linear regression, least absolute shrinkage selection operator (Lasso) models, generalized additive models (GAMs) analyze DAO/DAOA using 380...

10.1038/s41537-024-00548-z article EN cc-by-nc-nd Schizophrenia 2025-02-22

Genome-wide association studies and meta-analyses implicated that increased risk of developing Alzheimer's diseases (AD) has been associated with the ABCA7, APOE, BIN1, CASS4, CD2AP, CD33, CELF1, CLU, CR1, DSG2, EPHA1, FERMT2, HLA-DRB1, HLA-DRB4, INPP5D, MEF2C, MS4A4A, MS4A4E, MS4A6E, NME8, PICALM, PLD3, PTK2B, RIN3, SLC24A4, SORL1, ZCWPW1 genes. In this study, we assessed whether single nucleotide polymorphisms (SNPs) within these 27 AD-associatedgenes are linked cognitive aging...

10.18632/oncotarget.15269 article EN Oncotarget 2017-02-11
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