SMaHT at ASHG 2026

SMaHT Network members will present their research at the 2026 American Society of Human Genetics (ASHG) Annual Meeting. Explore the table below for a look at SMaHT presentations taking place throughout the meeting.

PresenterName of PresentationPresentation Type
Alexej AbyzovCharting Mutation Heterogeneity Across Human Tissues: Early Results from SMaHTPlenary (oral) Presentation
James BennettIdentification of Somatic Mutations in Surgically Resected Tissues from Individuals with Craniofacial Microsomia (CFM)Talk
Elliott SwansonSomatic Chromatin Epimutations Cap Genetic Determinism in the Human Diploid Chromatin EpigenomeTalk
Patrick Van HoosePediatric Pathology and Metadata Management for Biobanking CohortsTalk
Michelle NoyesUsing Fibroblast-Derived Donor Specific Assemblies to Call Somatic Mutation in a Haplotype-Resolved Manner- An Example of What You Can Do With a BiobankTalk
Thomas G. BlanchardA Neurobiobank Perspective: Challenges Associated with Brain Banking For Large Scale ProjectsTalk
Raquel G. HernandezDistinct Considerations for Deceased Donor Studies; Integration of Study TeamsTalk
Kathryn A. LawrenceFunctional Analysis of Somatic Variants Across Multiple Tissues in SMaHTLightning Talk + Poster
Andrew StergachisA Telomere-to-Telomere Map of Somatic Mutation BurdenPoster
Tara MackDonor-Specific Assemblies Enhance Somatic Structural Variant Detection Across Human TissuesPoster
David TangThe Landscape of Mosaic Chromosomal Alterations Across Human TissuesPoster
Flora VaccarinoGenetic, Genomic, and Epigenomic Resources and DatabasesPoster
Raquel G. HernandezDeveloping Genomic Donor Family Study Materials and Website Content with Stakeholder Input: Process and Lessons Learned from the ELSI 360 framework for the Somatic Mosaicism Across Human Tissues Study (SMaHT)Poster
Marie-Claude GingrasCross-Tissue SBS18 Enrichment in a monoallelic MUTYH p.Gly396Asp Carrier from the Somatic Mosaicism across Human Tissues (SMaHT) CohortPoster
Fritz SedlazeckA Multi-Tissue Atlas of Mosaic Structural Variation, Tandem Repeat Instability, and DNA Methylation Across Human TissuesPoster
Muchun NiuGenome-wide High-Precision Duplex-seq Enables the Identification of Tissue-Specific Somatic Mutational Signatures in Normal Tissues (CompDuplex)Poster
Yeongjun JangAccurate Detection of sub-1% Frequency Somatic Mutations by Whole Genome SequencingPoster