ASHG 2026 · Tier 1 Academic

University of Minnesota at ASHG 2026

Minneapolis, Minnesota

University of Minnesota at ASHG 2026 in Montréal: 15 presentations (13 posters, 1 platform talk, 1 lightning talk); 9 research groups.

15
presentations on the program
9
research groups identified
2
Reviewers’ Choice abstracts

Explore everyone at ASHG 2026 →

OrganizationASHG 2026 Attendance
University of Minnesota
Minneapolis, Minnesota
8 PhD Students · 3 Faculty · 2 PIs · 1 Staff Scientist
MCC Biostat Corectsi.umn.edu/services/statistical-support/meet-bdac-team
Dry lab~14 people
Provides statistical and data-management support for clinical trials from study design through publication. Works with the Masonic Cancer Center Biostat Core.
25 papers since 2024
Effects of stimulus size and contrast on binocular rivalry in adults with anisometropic amblyopia
Vision Research, 2025
Robust Small Area Estimation
Preprint or unlisted venue, 2025
Effects of electroacupuncture at "Fenglong"(ST40) and "Zusanli"(ST36) on the SIRT1/FOXO1 signaling pathway in non-alcoholic fatty liver disease model rats.
PubMed, 2025
Source: OpenAlex author A5060541476
8 platforms and techniques
Techniques
Survival analysis, Multistate models, Sparse regression, Bayesian statistics, Data integration, Causal inference, Monte-Carlo optimization, Machine learning
Source: lab pages
No funding stated · No openings posted
Talk
Wed Oct 21
2:15 pm
Interpretable multi-omic integration reveals novel epigenetic and transcriptomic subgroups in pancreatic ductal adenocarcinoma (PDAC)
Advancing Precision Oncology with AI, Functional Genomics, and Multi-Omics: From Risk Prediction to Tumor Evolution and Therapeutic Discovery
Collaborators: Mayo Clinic, University of Wisconsin–Eau Claire
CancerDeep learningGenomicsEpigenetics
Poster
Wed Oct 21
2:30 pm
★ Reviewers’ Choice
Interpretable Multi-Omic Integration Reveals Novel Epigenetic and Transcriptomic Subgroups in Pancreatic Ductal Adenocarcinoma (PDAC)
Cancer
Collaborators: Mayo Clinic, University of Wisconsin–Eau Claire
CancerDeep learningEpigeneticsGenomics
Poster
Fri Oct 23
2:30 pm
Estimating Total Mediation Effects of High-Dimensional Omics Mediators in Case-Control Studies
Statistical Genetics and Genetic Epidemiology
Collaborators: University of Virginia
GenomicsCardiovascular system
Division of Biostatistics and Health Data Sciencesph.umn.edu/academics/divisions/biostatistics/students
Dry lab~184 people
Develops statistical methods for smartphone, wearable-sensor and EHR data in biomedical research. Uses Bayesian analysis, machine learning and causal inference with University research partners.
12 platforms and techniques
Analyzes
smartphones, wearable sensors, administrative health databases (EHR), Olink NPX data
Techniques
Bayesian analysis, causal inference, statistical genetics & computational biology, machine learning, spatial statistics, survival analysis, functional data analysis, GWAS
Source: lab pages
No funding stated · No openings posted
Poster
Wed Oct 21
2:30 pm
Variance-based mediation analysis with mediator-exposure interactions for binary outcomes in cohort studies
Statistical Genetics and Genetic Epidemiology
Collaborators: University of Virginia
ProteomicsStatistical geneticsDiabetesEpidemiology
Poster
Wed Oct 21
2:30 pm
HierCELLX: A Hierarchical Bayesian Model for Interpretable Phenotype Prediction from Latent Cell Compositions in scRNA-seq
Artificial Intelligence and Machine Learning
Artificial intelligenceDiagnosticsMachine learningSingle-cell
Hsieh Labhsiehlab.umn.edu/people
Dry lab~6 people
Uses long-read sequencing and multi-omics biobank data with computational methods. Studies human evolution, adaptation and disease with the Human Pangenome Reference Consortium.
13 papers since 2024
A global view of human centromere variation and evolution
Nature, 2026
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus
Nature Genetics, 2024
Structural and genetic diversity in the secreted mucins MUC5AC and MUC5B
The American Journal of Human Genetics, 2024
Source: OpenAlex author A5061843819
Funded by NIH
NIH, K99/R00
“He received a PhD in Ecology and Evolutionary Biology from the University of Arizona and was a NIH K99/R00 fellow at the University of Washington.”
Source: lab pages
6 platforms and techniques
Analyzes
long-read sequencing, multi-omics biobank data
Techniques
phylogenetic methods, population genetic methods, statistical modeling, pangenome graph analysis
Source: lab pages
Currently hiring
“We welcome motivated trainees interested in computational and statistical approaches to study human genome function and evolution.”
Source: lab positions page
Talk
Wed Oct 21
11:00 am
Multi-ancestry selection and introgression maps in the NIH All of Us Biobank
Detecting Human Adaptation: Methods, Drivers, and Health Impacts of Natural Selection
Large-scale biobanksLong-read sequencingNatural selectionPopulation genetics
Poster
Fri Oct 23
2:30 pm
Enabling Polygenic Prediction from Structural Variants in the NIH All of Us Multi-Ancestry Biobank
Molecular Effects of Genetic Variation
Complex diseasesLarge-scale biobanksLong-read sequencingPolygenic risk score
Vrieze Labgenome.psych.umn.edu
Dry lab~1 people
Studies psychopathology and addiction with microarrays, whole genome sequencing and smartphone wireless sensors. Works through the Minnesota Center for Twin and Family Research.
39 papers since 2024
Mapping the genetic landscape across 14 psychiatric disorders
Nature, 2025
A deep catalogue of protein-coding variation in 983,578 individuals
Nature, 2024
Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk
JAMA Cardiology, 2024
Source: OpenAlex author A5019756851
Funded by National Institutes of Health, National Institute on Drug Abuse
National Institutes of Health, National Institute on Drug Abuse, T32 training grant in Genetic and Neurobehavioral Mechanisms of Addiction · active
“Fellows are supported by a T32 training grant funded by the National Institutes of Health’s National Institute on Drug Abuse.”
Source: lab pages
8 platforms and techniques
Works with
microarrays, whole genome sequencing, smartphone wireless sensors
Techniques
genetic association studies, twin/adoption studies, ecological momentary assessment, GPS location assessment, wireless-sensor assessments
Source: lab pages
Currently hiring
“We're currently accepting applications for talented postdoctoral fellows.”
Source: lab positions page
Poster
Fri Oct 23
2:30 pm
Cross-Ancestry Evaluation of Rare Variant Heritability for Complex Traits Using Whole Exome Sequencing
Complex Traits and Polygenic Disorders
Collaborators: Pennsylvania State University
Complex traitsHeritabilityLarge-scale biobanksRare variants
Poster
Fri Oct 23
2:30 pm
Gene-environment interplay in tobacco and alcohol use: Results from a global consortium.
Complex Traits and Polygenic Disorders
BehaviorGene environment interactionGenome-wide association study
Zaidi Labzaidilab.org
Dry lab~7 people
Uses theoretical modeling and empirical genomic data, including GWAS and mtDNA variation, to study human complex traits. Targets polygenic risk, admixture and mitochondrial disease genetics.
9 papers since 2024
Interpreting SNP heritability in admixed populations
Genetics, 2025
The multi-scale complexity of human genetic variation beyond continental groups
bioRxiv (Cold Spring Harbor Laboratory), 2024
Evaluation of Probiotic Bacteria Isolated from Indigenous Honeybee Species of Pakistan
Lahore Garrison University Journal of Life Sciences, 2024
Source: OpenAlex author A5047748699
Funded by NIH
NIH, MIRA award · active
“We received the NIH MIRA award. The lab is externally funded for the next five years!”
Source: lab pages
5 platforms and techniques
Techniques
Genome-wide association studies (GWAS), Theoretical modeling, Population genetic theory, Fine-mapping, Large-scale genomic and phenotypic data analysis
Source: lab pages
Currently hiring
“Interested applicants should email me directly”
Source: lab positions page
Poster
Wed Oct 21
2:30 pm
Tissue, not ancestry, mediates differences in the genetic and phenotypic architecture of mitochondrial DNA copy number across studies
Molecular Effects of Genetic Variation
Gene environment interactionGenome-wide association studyMitochondriaPhenome-wide association
Poster
Thu Oct 22
4:15 pm
Residual stratification and increased genetic diversity contribute to PGS prediction
Statistical Genetics and Genetic Epidemiology
Complex traitsGenome-wide association studyPolygenic risk scorePopulation structure
Advanced Research and Diagnostic Laboratory (ARDL)med.umn.edu/pathology/research/ardl/faculty
Wet lab~12 people
Runs immunoassay testing and mass spectrometry for clinical specimens, quantitative proteomics and assay validation. Supports NIH-sponsored trials and cohorts including NHANES, MESA and HRS.
Funded by NIH, NIH
NIH, multi-center clinical trials · active
“NIH-sponsored multi-center clinical trials”
NIH, CKiD Study · 2018-2023
“An NIH-funded, multicenter, prospective cohort study”
Source: lab pages
7 platforms and techniques
Runs
High-Volume Immunoassay Testing Platforms, Mass Spectrometer Center
Techniques
quantitative proteomics, assay development, assay validation, mass spectrometry, cell cryopreservation
Source: lab pages
No openings posted
Poster
Thu Oct 22
4:15 pm
Long read sequencing enables coordinated multi-scaled data analysis from large population studies: Findings from High School and Beyond and the Health and Retirement Study
Genetic, Genomic, and Epigenomic Resources and Databases
Collaborators: Columbia University, University of Wisconsin–Madison +2 more
Long-read sequencingEpigenetics
Anthropological Genetics Lab at UMNnievescolonlab.org
Wet lab~8 people
Uses ancient DNA and modern genomics to trace Caribbean and Latin American population history. Studies colonial encounters, Afro-descendant histories and health with descendant communities.
Funded by The Pew Charitable Trusts, UMN Urban Research and Outreach Engagement Center +3 more
UMN Urban Research and Outreach Engagement Center, Dr. Josie R. Johnson Dissertation Fellowship · 2026
“awarded a 2026 Dr. Josie R. Johnson Dissertation Fellowship from the UMN Urban Research and Outreach Engagement Center.”
The Pew Charitable Trusts, Pew Scholars Program in the Biomedical Sciences · 2025
“The Pew Charitable Trusts today announced the 22 researchers joining the Pew Scholars Program in the Biomedical Sciences”
National Science Foundation, Doctoral Dissertation Research Improvement Grant (DDRIG) · 2025
“received grant funding from the National Science Foundation Doctoral Dissertation Research Improvement Grant (DDRIG)”
+2 more on the lab page
Source: lab pages
11 platforms and techniques
Runs
Ancient DNA cleanroom, Molecular Genetics Laboratory, Mixer Mill, Fluorometer, Thermal cyclers
Techniques
Ancient DNA analysis, Y-chromosome enrichment, DNA methylation, Geometric morphometrics, 3D scanning, Mitochondrial DNA analysis
Source: lab pages
No openings posted
Poster
Fri Oct 23
2:30 pm
Reconstructing Afro-Peruvian genomic histories across three centuries through community-engaged research
Evolutionary and Population Genetics
Collaborators: National University of San Marcos, Erasmus Student Network AISBL
Ancient DNAMitochondriaPopulation structurePopulation genetics
Center for Childhood Cancer Genomics (CCCG)cccg.umn.edu
~27 people
Analyzes population-genomics, GWAS, exome-wide and case-control/case-parent datasets from pediatric cancers. Uses them for risk prediction, early detection and prevention.
71 papers since 2024
The landscape of primary mismatch repair deficient gliomas in children, adolescents, and young adults: a multi-cohort study
The Lancet Oncology, 2024
In Utero Origins of Acute Leukemia in Children
Biomedicines, 2024
Sex differences in osteosarcoma survival across the age spectrum: A National Cancer Database analysis (2004–2016)
Cancer Epidemiology, 2024
Source: OpenAlex author A5054442842
Funded by Children’s Cancer Research Fund
Children’s Cancer Research Fund · 2020
“The Childhood Cancer Genomics Group was founded in 2020 by Dr. [name] with a foundational gift from the Children’s Cancer Research Fund.”
Source: lab pages
6 platforms and techniques
Techniques
population genomics, integrative genomic analyses, family-based studies, mutational epidemiology, gene-by-environment interactions, exome-wide investigation
Source: lab pages
No openings posted
Poster
Fri Oct 23
2:30 pm
Multiancestry GWAS identifies variants near BCL11A, FST, and 8q24 in development of the rare pediatric liver cancer hepatoblastoma
Cancer
Collaborators: Hiroshima University, Ludwig-Maximilians-Universität München +5 more
CancerGenome-wide association studyDevelopmentPolygenic risk score
Koob Lab
Works in computational genetics.
Poster
Fri Oct 23
2:30 pm
★ Reviewers’ Choice
TMEM106B Protective Haplotype is Associated with Higher Populations of an Excitatory Neuron Subtype
Molecular Effects of Genetic Variation
Alzheimer’s diseaseBioinformaticsGenotype-phenotype correlationsSingle-cell

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