Companies at ASHG 2026
Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website
268 companies are at ASHG 2026 — 330 presentations on the program and 163 with a booth in the exhibit hall. Most represented: Illumina (19 on the program), LabCorp (19 on the program), Ambry Genetics (11 on the program). 168 of them have their own page in this guide. As of Sep 25, 2026.
Scientific focus
Top represented
Showing 1–2 of 268 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 |
LabCorp Burlington, Vermont | 1 Lab Director · 1 Senior Applied Research Scientist in Oncology · 1 Data scientist · 1 Statistical Geneticist · 4 other presenters |
Labcorp is a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions.
| Booth Exhibiting at Booth 1024 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Session Wed Oct 21 1:30 pm Talk Wed Oct 21 1:43 pm Poster Wed Oct 21 2:30 pm Diagnostic Yield and Clinical Utility of Genetic Testing in Unaffected Relatives with a Family History of Sudden Cardiac Death Genetic testingCardiovascular systemChannelopathiesClinical genetics Poster Wed Oct 21 2:30 pm Preoperative Lynch syndrome diagnosis and surgical outcomes in colorectal cancer: Evaluating resection extent, post-operative complications, and rates of metachronous and other cancers CancerGenetic testingPublic healthCancer syndromes Poster Wed Oct 21 2:30 pm Retrospective virtual panel modeling of carrier and high-risk couples detection by panel size in a large clinical reproductive carrier screening cohort Clinical testingGenetic counselingReproductive geneticsWomen's health Poster Wed Oct 21 2:30 pm ★ Reviewers’ Choice Sex-driven gaps in guideline-concordant follow-up after population genomic screening for hereditary cancer, cardiovascular, and metabolic conditionsGenetic testingCancer syndromesGenetic epidemiologyPrecision medicine Poster Wed Oct 21 2:30 pm From global calibration to gene-aware evidence: calibrating pathogenicity predictions for real-world variant interpretation Artificial intelligenceVariant interpretationMethodologyGenetic testing Poster Wed Oct 21 2:30 pm ★ Reviewers’ Choice Ancestry‑wide analysis of real‑world genomic testing reveals clinically relevant disparities in cancer prevalence, immunotherapy biomarkers, and variant actionabilityCancerClinical testingDiagnosticsEpidemiology Talk Thu Oct 22 8:15 am Closing the equity gap in variant classification: Machine learning-driven evidence demonstrates differential impact across race and ethnicity Computational toolsEthical, legal, and social implicationsGenetic testingMachine learning Talk Thu Oct 22 11:30 am Talk Thu Oct 22 2:15 pm Surveying the structural variant landscape in genetic testing: Prevalence and diagnostic yield in a clinical cohort of 1.8 million individuals Clinical geneticsCopy number/structural variationDiagnosticsGenetic testing Poster Thu Oct 22 4:15 pm ★ Reviewers’ Choice The impact of an iterative points-based framework on variant classification outcomes for neurodevelopmental disorders.Artificial intelligenceVariant interpretationNeurodevelopmentalClinical testing Poster Thu Oct 22 4:15 pm Applying Single Cell Transcriptomics and Machine Learning to Classify SCN1A Variants According to Disease Mechanism Laboratory genetics and genomicsGenomicsMachine learningGenetic variation Poster Thu Oct 22 4:15 pm A machine learning framework for accurate SMN1 copy number determination from short-read next-generation sequencing data BioinformaticsCopy number/structural variationGenomicsMachine learning Poster Thu Oct 22 4:15 pm Biochemical data and genetic testing: combining datasets to help classify variants Laboratory genetics and genomicsVariant interpretationPhenotypeMetabolic disorder Poster Fri Oct 23 2:30 pm Assessment of Structural and Copy Number Variants in Constitutional Samples Using Electronic Genome Mapping AneuploidyChromosomal abnormalitiesClinical testingCopy number/structural variation Poster Fri Oct 23 2:30 pm Validating gain- and loss-of-function multiplexed assay of variant effect (MAVE) predictions using linked genetic testing and biochemical datasets: a CASR case study Variant interpretationGenotype-phenotype correlationsMendelian disorderRare variants Poster Fri Oct 23 2:30 pm Evidence supporting RPS20 as a colorectal cancer susceptibility gene from a case-control study CancerCancer syndromesGenetic epidemiologyGenetic testing Poster Fri Oct 23 2:30 pm A conversational AI agent for multi-domain clinicogenomic research analytics with layered human-in-the-loop verification Artificial intelligenceComputational toolsDatabasesGenotype-phenotype correlations Poster Fri Oct 23 2:30 pm Single-cell transcriptomic variant effect mapping of clinically relevant MSH3 variants Machine learningMassively parallel sequencingVariant interpretation |
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