Join us at ASHG 2026 to learn how the Illumina Insight Ecosystem is helping researchers connect genomic data and insights to advance discovery.
Visit Illumina booth 701 and attend our Industry Education sessions and Co-Labs to hear more about our products, workflow solutions, and partnerships.
Wednesday, October 21
12:15 PM–1:15 PM (ET)
Room 512 ABCEFG
Thursday, October 22
12:15 PM–1:15 PM (ET)
Room 512 ABCEFG
Friday, October 23
12:15 PM–1:15 PM (ET)
Room 513 ABC
Thursday, October 22
4:15 PM–4:45 PM (ET)
Theater 1, Exhibit Hall
Friday, October 23
2:30 PM–3 PM (ET)
Theater 1, Exhibit Hall
Thursday, October 22
6:30 PM–9 PM (ET)
Humaniti Hotel Montreal
340 Rue De la Gauchetière O O, Montreal, QC
| Title | Authors | Poster # |
|---|---|---|
| 3D tissue reconstruction using Illumina Spatial Technology reveals the predicted preservation of the senescence programs in human benign nevocellular nevus | Mark Wang, Kareem Ahmad/Kevin Thai | |
| Enabling small-scale Illumina Transcriptomics Technology workflow for benchtop sequencing platforms | Darren Segale, Kareem Ahmad | |
| Multiplexed high-throughput NGS-based proteomics assay using CSF and cell or tissue lysates optimized for discovery and translational research | Fiona Kaper, Andrew Slatter | |
| High accurate methlyation profiling and whole genome sequencing in FFPE sample types | Cande Rogert, Lisa Watson | |
| Targeted profiling of CYP2D6, CYP2B6 and CYP21A2 in an integrated exome-based NGS workflow | Severine Catreux, Eric | |
| Significant optimization of sequencing performance T2T genomes, including long homopolymers via modification of reaction conditions for sequencing | Carolyn Conant | |
| Proximity-informed structural variant detection with Illumina TruPath Genome | James Han, Sean | |
| Inter-individual multiomics improves subtype resolution and risk stratification in cardiovascular disease | Yongwen | |
| Adapting Illumina Single Cell 3' RNA Kit for 3' Single Cell V(D)J enrichment: Enabling paired TCR α/β recovery on the MiSeq i100 Plus | Robert Meltzer, Robin Bombardi | |
| Research method for whole-chromosome uniparental disomy (UPD) detection with DRAGEN secondary analysis software | Khodor Hannoush, Fabian Klotzl, Konrad Scheffler, Shyamal Mehtalia |