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

Explore everyone at ASHG 2026 →

OrganizationASHG 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
Public company~8,600 people
Illumina sells DNA sequencing and array-based technologies. It serves research, clinical, and applied-market customers.
Illumina's Billion Cell Atlas alliance added AI-native drug developer Formation Bio and other members, widening its AI-biopharma customer reach.
Illumina's Billion Cell Atlas alliance added AI-native drug developer Formation Bio and other members, widening its AI-biopharma customer reach.
2026-07 · source
Illumina appointed Sullivan and Coletti to its executive leadership team, adding experienced decision-makers you may now be selling to.
2026-07 · source
Illumina launched StrataMap Spatial, a new whole-transcriptome spatial platform, giving customers an in-house option instead of buying elsewhere.
2026-06 · source
Source: company newsroom
Q2 2026 revenue $1.16B, up 9.5%
FY2026 guidance raised to $4.60-$4.64 billion, signaling steady growth and budget for sequencing purchases. · 2026-07-30
“Revenue of $1.16 billion for Q2 2026, up 9.5% from Q2 2025. For fiscal year 2026, we now expect total revenue of $4.60-$4.64 billion.”
Source: results release
Currently hiring
Source: careers page
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
Plenary Abstract Session I
Collaborators: University of Oxford, Queen Mary University of London +1 more
Artificial intelligenceBioinformaticsVariant interpretationGenotype-phenotype correlations
Poster
Wed Oct 21
2:30 pm
Proximity-informed structural variant detection with Illumina TruPath Genome
Omics Technologies
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
Omics Technologies
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
Genetic Therapies and Precision Medicine
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
Omics Technologies
MethylationGenomicsExome/genome sequencingEpigenetics
Poster
Fri Oct 23
2:30 pm
Enabling flexible small-scale Illumina Spatial Technology workflow for benchtop sequencing platforms
Omics Technologies
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
Laboratory Genetics and Genomics
Collaborators: Boston Children's Hospital
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
Omics Technologies
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
Pharmacogenomics
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
Prenatal, Perinatal, Reproductive, and Developmental Genetics
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
Complex Traits and Polygenic Disorders
Collaborators: Henry Ford Health
Multi-omicsCardiovascular systemGene regulationMachine learning

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