2025
SuperGLUE facilitates an explainable training framework for multi-modal data analysis
Liu T, Zhao J, Zhao H. SuperGLUE facilitates an explainable training framework for multi-modal data analysis. Cell Reports Methods 2025, 5: 101167. PMID: 40914154, DOI: 10.1016/j.crmeth.2025.101167.Peer-Reviewed Original ResearchMeSH KeywordsAlgorithmsComputational BiologyData AnalysisDeep LearningGene Regulatory NetworksHumansSingle-Cell AnalysisConceptsData integrationProbabilistic deep learningMulti-modal data analysisInference of gene regulatory networksMulti-modal data integrationDeep learningGene regulatory networksTraining frameworkBaseline modelRegulatory networksComplex biological systemsRegulatory relationshipsSensing dataCell statesGlobal structureArea of active researchActive researchOmicsBiological featuresScalable methodFrameworkBiological systemsStatistical modelNetworkBiological linkagesscMODAL: a general deep learning framework for comprehensive single-cell multi-omics data alignment with feature links
Wang G, Zhao J, Lin Y, Liu T, Zhao Y, Zhao H. scMODAL: a general deep learning framework for comprehensive single-cell multi-omics data alignment with feature links. Nature Communications 2025, 16: 4994. PMID: 40442129, PMCID: PMC12122792, DOI: 10.1038/s41467-025-60333-z.Peer-Reviewed Original ResearchConceptsDeep learning frameworkSingle-cell multi-omics researchSingle-cell multi-omics dataLearning frameworkMulti-omics dataGenerative adversarial networkSingle-cell technologiesData alignmentSingle-cell resolutionMulti-omics researchDownstream analysisCellular statesOmics datasetsAdversarial networkNeural networkProteomic profilingCorrelated featuresBiological informationOmics perspectiveDiverse datasetsFeature topologyDisease mechanismsCell embeddingData resourcesRelationship inference
2024
Enhancing patient representation learning with inferred family pedigrees improves disease risk prediction
Huang X, Arora J, Erzurumluoglu A, Stanhope S, Lam D, Arora J, Erzurumluoglu A, Lam D, Khoueiry P, Jensen J, Cai J, Lawless N, Kriegl J, Ding Z, de Jong J, Zhao H, Ding Z, Wang Z, de Jong J. Enhancing patient representation learning with inferred family pedigrees improves disease risk prediction. Journal Of The American Medical Informatics Association 2024, 32: 435-446. PMID: 39723811, PMCID: PMC11833479, DOI: 10.1093/jamia/ocae297.Peer-Reviewed Original ResearchConceptsElectronic health recordsDisease risk predictionElectronic health record researchFamily health historyGenetic aspects of diseaseRisk predictionInflammatory bowel disease subtypeHealth recordsHealth historyAspects of diseaseFamily relationsHealthcare ResearchPatient's disease riskInfluence of geneticsDisease riskDiagnosis dataFamily pedigreeEnvironmental exposuresRisk factorsDisease dependencyPatient representation learningClinical profileFamilyDisease subtypesRisk
2023
scNAT: a deep learning method for integrating paired single-cell RNA and T cell receptor sequencing profiles
Zhu B, Wang Y, Ku L, van Dijk D, Zhang L, Hafler D, Zhao H. scNAT: a deep learning method for integrating paired single-cell RNA and T cell receptor sequencing profiles. Genome Biology 2023, 24: 292. PMID: 38111007, PMCID: PMC10726524, DOI: 10.1186/s13059-023-03129-y.Peer-Reviewed Original Research
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