University of California, Santa Cruz at ASHG 2026
Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website
University of California, Santa Cruz brings 4 presentations from 4 research groups to ASHG 2026 in Montréal, and exhibits at Booth 320. Its program at this meeting centres on rare disease, cancer, and population genetics through computational genomics. The Cornejo Lab brings ancestry analysis beyond geographic labels, the Genomics Institute brings Varaico’s literature-based variant collection, and the Haussler-Salama Lab brings a haplotype-phased H9 genome assembly.
| Organization | ASHG 2026 Attendance |
|---|---|
University of California, Santa Cruz Santa Cruz, California | 2 PIs · 1 PhD Student |
Booth Exhibiting at Booth 320 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm | |
Cornejo Labourgenomes.sites.ucsc.edu Studies genomes from humans, microbiomes, malarial parasites and plants using long-read sequencing and hybrid capture. Focuses on host-microbe evolution, disease resistance and HLA haplotyping.
| Poster Wed Oct 21 2:30 pm Ancestry analysis of International Histocompatibility Working Group cell lines: beyond geographic labels Population geneticsPopulation structureImmune system |
Genomics Instituteucscgenomics.soe.ucsc.edu Builds genomic data platforms and tools including Dockstore, BioData Catalyst, AnVIL and Human Cell Atlas access. Applies genomics to human health and species conservation.
| Poster Wed Oct 21 2:30 pm Varaico update collects genetic variants from full-text literature and supplementary data (www.varaico.com) Variant interpretationGenetic testingExome/genome sequencingDiagnostics |
Haussler-Salama Labstemcellgenomics.ucsc.edu/people/members-of-the-lab Uses pluripotent stem cells, cerebral cortex organoids, CRISPR and single-cell RNA-seq. Studies primate brain evolution, neurodevelopmental disease and pediatric glioma.
| Poster Fri Oct 23 2:30 pm Resolving the H9 Genome: A T2T Haplotype-Phased Assembly Unlocks Allele-Specific Insights GenomicsStem cellSequencing technologyPrecision medicine |
Miga Labmigalab.com Produces nanopore long-read data for telomere-to-telomere chromosome assemblies and epigenetic maps. Studies satellite DNA variation in human centromeres and disease.
| Talk Thu Oct 22 9:00 am The Human Pangenome Project:
A new foundation for human genomics Clinical geneticsEthical, legal, and social implicationsEvolutionary geneticsGenomics |
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