Instrument and reagent vendors at ASHG 2026
Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website
49 instrument and reagent vendors are at ASHG 2026 — 84 presentations on the program and 34 with a booth in the exhibit hall. Most represented: Illumina (19 on the program), PacBio (6 on the program), Genomics (5 on the program). 34 of them have their own page in this guide. As of Sep 25, 2026.
Scientific focus
Top represented
Showing 1–5 of 49 organizations
| Organization | ASHG 2026 Attendance |
|---|---|
Illumina San Diego, California | 1 Senior Manager · 1 Vice President and Global Head of Advanced Science · 1 Sr Director, R&D · 1 Sr Director, Scientific Research-Advanced Platforms · 1 other presenter |
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 Session Tue Oct 20 10:00 am Session Tue Oct 20 1:00 pm 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 Wed Oct 21 2:30 pm A unified deep learning framework for quantitative splicing and transcript prediction Alternative splicingArtificial intelligenceDeep learningGenomics Poster Wed Oct 21 2:30 pm Reverse-engineering genetic architecture of human diseases from 1.3M human genomes with EHR data Phenome-wide associationGenotype-phenotype correlationsRare variantsComplex traits Poster Wed Oct 21 2:30 pm Impact of CYP2D6 Allele Content on Metabolizer Phenotype Assignment: Contribution of AMP Tier 2 Alleles to Phenotype Concordance PharmacogenomicsPopulation geneticsPrecision medicine Session Wed Oct 21 2:45 pm 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 Significant optimization of sequencing performance for T2T genomes, including long homopolymers via modification of reaction conditions for sequencing. Triplet and other repeatsCopy number/structural variationExome/genome sequencingGenetic mapping 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 Advancing Whole-Exome Sequencing Through Optimized Coverage and Enrichment Performance Exome/genome sequencingLaboratory genetics and genomicsGenetic testingGenomics 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 |
PacBio Menlo Park, California | 1 Senior Product Manager, PacBio · 1 Bioinformatics Scientist · 1 Scientist · 1 Principal I Scientist, Bioinformatics · 1 other presenter |
PacBio sells HiFi long-read sequencing systems, consumables, sample-prep kits, and analysis software to scientists and clinical researchers.
| Booth Exhibiting at Booth 605 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Poster Wed Oct 21 2:30 pm One-hour automated HMW DNA extraction from blood and saliva for HiFi sequencing Laboratory genetics and genomicsLong-read sequencingMethodologySequencing technology Poster Wed Oct 21 2:30 pm Long-read sequencing identifies and refines genome-wide methylation signals in multiple tumor types BioinformaticsCancerEpigeneticsEpigenome-wide association studies Poster Thu Oct 22 4:15 pm Kinnex-IsoSeq-WDL: Workflows for High Throughput Analysis of HiFi Kinnex Full-Length RNA Data BioinformaticsRNALong-read sequencingTranscriptome Poster Thu Oct 22 4:15 pm ★ Reviewers’ Choice Towards rapid HiFi long-read whole genome sequencing for time-critical rare disease applicationsLong-read sequencingSequencing technologyExome/genome sequencingDiagnostics Poster Thu Oct 22 4:15 pm Resolution of the D4Z4 repeat responsible for facioscapulohumeral muscular dystrophy with HiFi sequencing Long-read sequencingClinical geneticsCopy number/structural variationMuscular abnormalities Poster Fri Oct 23 2:30 pm Simultaneous genetic and epigenetic profiling of the human genome at single-base resolution with PacBio HiFi sequencing MethylationDeep learningMulti-omicsChromatin |
Genomics Oxford, UK | 1 Scientist · 1 Bioinformatician · 1 Chief Scientific Officer · 1 Research Scientist · 1 other presenter |
Genomics sells AI-enabled human-genetics analytics and polygenic-risk testing to biopharma and healthcare providers.
| Booth Exhibiting at Booth 1418 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Poster Wed Oct 21 2:30 pm ★ Reviewers’ Choice A machine learning framework for genome-wide signal-to-gene mapping achieves state-of-the-art causal gene prioritisationMachine learningArtificial intelligenceGenomicsMulti-omics Poster Wed Oct 21 2:30 pm A Genetics-First Framework for Predicting On-Target Safety Liabilities GenomicsMachine learningPharmacogenomicsStatistical genetics Poster Thu Oct 22 4:15 pm ★ Reviewers’ Choice Our Future Health: Emerging genetic insights from the world’s largest health research programmeDatabasesGenome-wide association studyPolygenic risk scorePopulation structure Poster Thu Oct 22 4:15 pm Improved multi-trait colocalisation using MTColoc Complex traitsComputational toolsExpression quantitative trait lociGenome-wide association study Poster Fri Oct 23 2:30 pm ★ Reviewers’ Choice Evaluation of a novel AI agent for statistical genetics and target discoveryArtificial intelligenceStatistical genetics |
Oxford Nanopore Technologies New York, New York | 2 Principal Applications Bioinformatician · 1 Senior Bioinformatician, Commercial Applications · 1 Senior Director of Commercial Applications · 1 Associate Director, Genomic Applications Bioinformatics |
Oxford Nanopore sells real-time DNA/RNA sequencing devices, flow cells, and analysis software. Its customers include research, clinical, and biopharma teams.
| Booth Exhibiting at Booth 901 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Poster Wed Oct 21 2:30 pm ★ Reviewers’ Choice Large population-scale WGS with Oxford Nanopore Sequencing in UK BiobankLong-read sequencingCopy number/structural variationGenomicsMethylation Poster Wed Oct 21 2:30 pm Profiling the Structure and Epigenetics of D4Z4 Arrays in FSHD Using Oxford Nanopore Sequencing BioinformaticsLong-read sequencingMethylationMulti-omics Poster Wed Oct 21 2:30 pm Hybridization-capture enrichment and full-length single-cell TCR profiling using Oxford Nanopore sequencing Immune systemLong-read sequencingSingle-cellTargeted sequencing Poster Thu Oct 22 4:15 pm Evaluation of Oxford Nanopore whole genome methylation sequencing for phenotype inference and association testing EpigeneticsLong-read sequencingEpigenome-wide association studiesMethylation Poster Fri Oct 23 2:30 pm ★ Reviewers’ Choice Beyond standard variant calling: analysis tools for resolving challenging medically relevant genes using nanopore whole-genome and digital panel dataBioinformaticsComputational toolsCopy number/structural variationTargeted sequencing |
Agilent Technologies Santa Clara, California | 2 R&D Scientist · 1 Product Marketing Director · 1 Product Manager |
Agilent sells instruments, software, and consumables to laboratories. It also provides genomics assays, sample QC, and workflow services for research and diagnostics.
| Booth Exhibiting at Booth 1017 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Poster Wed Oct 21 2:30 pm Low-input gDNA integrity assessment for FFPE specimens using a multi-tissue sample set GenomicsLarge-scale biobanksLaboratory genetics and genomics Poster Wed Oct 21 2:30 pm Poster Wed Oct 21 2:30 pm A Scalable PCR- Free WGS Workflow Enabling Accurate Library Quantification and Improved Coverage Across Sequencing Platforms Variant callingSNP analysis/discoveryGenomicsExome/genome sequencing Poster Wed Oct 21 2:30 pm Next Generation Multiplex Hybrid Capture and Sequencing Enabled by Workflow Integration and Enhanced Library Complexity Sequencing technologyTargeted sequencingExome/genome sequencing |
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