Oxford Nanopore at ASHG 2026
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Oxford Nanopore will be at the ASHG Annual Meeting at Booth 901 in October, 2026, hosted in Montreal. We will also host a Industry Education Session on Wednesday, 21 October, and 2 CoLabs on Thursday, October 22nd. See additional details below.
Industry Education Session
Date: Wednesday, October 21
Time: 3:00–4:00 PM
Location: Room 512 A-G
Speaker details and registration coming soon.
Agenda
3:00–4:00 PM EST | Talk title | Speaker |
|---|---|---|
3:00–3:05 PM | Welcome and introductions | Cora Vacher, Oxford Nanopore Technologies |
3:05–3:30 | From variant to haplotype: long-read sequencing across Mendelian disease and cancer | Debarshi Mustafi, University of Washington |
3:30 - 4:00 | Oxford Nanopore Technologies Update | Oxford Nanopore Technologies |
CoLabs
Oxford Nanopore will be hosting two CoLabs at the ASHG 2026 annual meeting. CoLabs are 30-minute sessions hosted in the exhibit hall to showcase offerings from our industry experts and thought leaders. View session details below and register to attend.
CoLab 1
Location: CoLab Theater 1
Date: Thursday, October 22
Time: 1:00 — 1:30 PM EDT
CoLab details TBC
CoLab 2: Unlocking difficult-to-resolve genomic regions with long reads and dedicated tools
Location: CoLab Theater 2
Date: Thursday, October 22
Time: 5:45 – 6:16 PM EDT
Oxford Nanopore information-rich data is opening new possibilities for resolving challenging regions of the human genome. The long-range information can span repeat-rich and highly homologous sequence, while native methylation information is retained in the underlying data. This session will explore how dedicated analysis and visualisation tools make the most of these capabilities, supporting comprehensive characterisation of complex genes and repeat expansions. The speakers will show how Oxford Nanopore long-read data can be used to detect a broad range of variant types, resolve repeat structure and allele-specific variation, and distinguish genes from pseudogenes and paralogues. The same analysis approach can be applied across whole-genome sequencing and targeted workflows enabled by Adaptive Sampling, giving researchers flexibility to investigate the regions most relevant to their work. Join us to learn how Oxford Nanopore sequencing and dedicated tools can extend genomic analysis beyond the regions that standard approaches often struggle to characterise in research and clinical genomics.
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Registration details to come soon.
