ASHG 2026 · Tools, software & services

Helix at ASHG 2026

San Mateo, California

Helix at ASHG 2026 in Montréal: 8 presentations (5 posters, 2 platform talks, 1 plenary); Booth 1200.

8
presentations on the program
1200
exhibit booth

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OrganizationASHG 2026 Attendance
Helix
San Mateo, California
2 Senior Research Scientist · 1 Medical Director · 1 Associate Director Research · 1 Senior Staff Scientist
Private company
Helix sells population-scale genomic testing, clinico-genomic data, and research tools to health systems and life-science companies.
Helix signed a multi-year deal giving AstraZeneca access to its growing, deeply phenotyped GenoSphere cohorts for drug discovery research.
Helix signed a multi-year deal giving AstraZeneca access to its growing, deeply phenotyped GenoSphere cohorts for drug discovery research.
2026-07 · source
Helix launched a GenoSphere MCP connector inside Claude Science, making its genomic data directly accessible through AI tools.
2026-07 · source
Nebraska Medicine and Memorial Hermann launched Helix Genomic Advantage, a new population health system partnership improving care and lowering cost.
2026-06 · source
Source: company newsroom
Raised $50M Series C (Jun 2021)
Led by Warburg Pincus, DFJ Growth, Kleiner Perkins, Mayo Clinic, and Temasek; most recent disclosed round. · 2021-06-03
“The $50M round will be used to accelerate the organization's population genomics platform.”
Source: funding announcement
Booth
Exhibiting at Booth 1200
Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm
Plenary
Tue Oct 20
5:57 pm
Population genomic screening for CDC Tier 1 conditions drives guideline-concordant care across 428,626 participants from 13 health systems
Plenary Abstract Session I
Collaborators: Memorial Hermann, Clinical Research Institute +11 more
Genetic testingPopulation geneticsClinical geneticsPrecision medicine
Talk
Wed Oct 21
11:45 am
Distinct genetic architectures of kidney function decline quantified by multi-state Markov analysis of 3.4 million serial eGFR measurements across 13 health systems
The REnAL Deal: Genomic Insights into Kidney Disease
Complex traitsGenetic epidemiologyGenotype-phenotype correlationsPolygenic risk score
Talk
Thu Oct 22
1:45 pm
Rare GLP1R variants selectively attenuate weight loss with semaglutide but not tirzepatide, implicating GIP receptor agonism as a compensatory mechanism
Leveraging Pharmacogenomics for Drug Trial-Level Evidence
PharmacogenomicsRare variantsObesityPrecision medicine
Poster
Thu Oct 22
4:15 pm
APOE genotype shapes the trajectory from mild cognitive impairment to dementia in a large clinical genomics cohort
Complex Traits and Polygenic Disorders
NeurodegenerationElectronic health recordsGenotype-phenotype correlationsPrecision medicine
Poster
Thu Oct 22
4:15 pm
ApoB isoform-specific mechanisms of liver disease in heterozygous pLoF carriers across three population cohorts
Molecular Effects of Genetic Variation
Collaborators: University of Nevada, Reno
Clinical geneticsGenetic variationLarge-scale biobanks
Poster
Fri Oct 23
2:30 pm
Plasma proteomics highlights a preclinical cardiomyopathy signature in pathogenic variant carriers without clinical diagnosis
Artificial Intelligence and Machine Learning
Cardiovascular systemMachine learningProteomicsRare variants
Poster
Fri Oct 23
2:30 pm
Plasma proteomic signatures of kidney disease within APOL1 genotype strata in a population genomic screening program
Complex Traits and Polygenic Disorders
Clinical testingGenetic testingMetabolic disorderPrecision medicine
Poster
Fri Oct 23
2:30 pm
Cumulative pharmacogenomic variant burden associates with polypharmacy, treatment inefficacy, and adverse drug events
Pharmacogenomics
Collaborators: St. Luke's University Health Network
PharmacogenomicsPharmacologic therapyGenetic variationGenotype-phenotype correlations

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