ASHG 2026 · Tools, software & services
Illumina at ASHG 2026
San Diego, California
Illumina at ASHG 2026 in Montréal: 12 presentations (11 posters, 1 plenary); Booth 701.
12
presentations on the program
701
exhibit booth
| Organization | ASHG 2026 Attendance |
|---|---|
Illumina San Diego, California | 1 Senior Manager · 1 Vice President and Global Head of Advanced Science · 1 Sr Director, Scientific Research-Advanced Platforms · 1 Vice President, Systems Integration & Solutions |
Illumina sells DNA sequencing and array-based technologies. It serves research, clinical, and applied-market customers.
| Booth Exhibiting at Booth 701 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Plenary Tue Oct 20 5:00 pm Automated interpretation of rare disease genomes with deep graph attention Artificial intelligenceBioinformaticsVariant interpretationGenotype-phenotype correlations Poster Wed Oct 21 2:30 pm Proximity-informed structural variant detection with Illumina TruPath Genome Copy number/structural variationGenomic structureSequencing technology Poster Thu Oct 22 4:15 pm Poster Thu Oct 22 4:15 pm 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 Alternative splicingSingle-cellImmune systemTranscriptome Poster Thu Oct 22 4:15 pm Reliable detection of uniparental disomy from trio sequencing data using chromosome scale inheritance patterns BioinformaticsClinical geneticsCopy number/structural variationChromosomal abnormalities Poster Fri Oct 23 2:30 pm A streamlined method for simultaneous, high accurate methylation profiling and whole genome sequencing in FFPE sample types MethylationGenomicsExome/genome sequencingEpigenetics Poster Fri Oct 23 2:30 pm Enabling flexible small-scale Illumina Spatial Technology workflow for benchtop sequencing platforms Multi-omicsNon-coding RNARNASpatial transcriptomics Poster Fri Oct 23 2:30 pm Resolving challenging genes for nonsyndromic sensorineural hearing loss using on flowcell proximity sequencing Sequencing technologyVariant callingCopy number/structural variationLaboratory genetics and genomics Poster Fri Oct 23 2:30 pm Multiplexed high throughput NGS based proteomics assay using CSF and cell or tissue lysates optimized for discovery and translational research Brain/nervous systemMassively parallel sequencingMulti-omicsProteomics Poster Fri Oct 23 2:30 pm Targeted Profiling of CYP2D6, CYP2B6 and CYP21A2 in an Integrated Exome-Based NGS Workflow Clinical testingComputational toolsCopy number/structural variationExome/genome sequencing Poster Fri Oct 23 2:30 pm Clinical laboratory experience with paired‑end sequencing–based noninvasive prenatal screening for 22q11.2 deletion: A retrospective analysis BioinformaticsCell-free DNACopy number/structural variationNIPT Poster Fri Oct 23 2:30 pm Inter-individual multiomics improves subtype resolution and risk stratification in cardiovascular disease Multi-omicsCardiovascular systemGene regulationMachine learning |
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