Geneyx Genomex Ltd. | Company Profile - Revenue, Headcount, Tech Stack, Contacts
Company Directory for Geneyx Genomex Ltd.
Geneyx Genomex Ltd.
Overview
Geneyx Genomex Ltd. is a Delaware-based genomics company founded in 2018. It specializes in next-generation sequencing (NGS) data analysis and clinical genetic interpretation. With a mission to integrate genomics into healthcare and pharmaceutical research, it has a global presence, operating in 190 hospitals and labs across 50 countries and analyzing over 520,000 samples.
The company offers advanced technologies such as HiFi long-read sequencing and Sequencing by Binding (SBB™) short-read technology. Its primary product, Geneyx Analysis, is a leading platform for NGS interpretation, used for secondary and tertiary analysis of exome and whole genome sequencing. In addition to clinical interpretation services and pharmacogenomics insights, their unique Phenotyper® technology enhances diagnostic yields. The platform supports human genetics, oncology, and microbiology applications, serving hospitals, life-science companies, and pharmaceutical research organizations. Geneyx has been recognized as one of the World's Best Digital Health Companies for 2024.
Basic Information
| Industry | research |
|---|---|
| Founded | 2018 |
| Revenue | 5M |
| Headquarters | 11 Galgale Haplada St., Entrance B 2nd Floor, Herzliya, Tel Aviv District, Israel 4672211 |
Contact Details
- Website: geneyx.com
- LinkedIn: linkedin.com/company/geneyxgenomex
Key Focus Areas & Initiatives
- Cardiogenetics
- WES data analysis
- NGS analysis
- Clinical genetic data
- Clinical genetic data integration
- Therapeutics discovery
- Target research
- Genome base diagnostics
- NGS longreads
- WGS data analysis
- AI driven tertiary analysis
- Rare diseases
- Genetic data
- Hereditary diseases
- Genetic data interpretation
- Phenotypegenotype association
- Biotechnology research
- AI-based genetic data analysis
- Structural and copy number variation analysis
- Clinical genetic interpretation
- Rare disease diagnosis
- Genomic data analysis
- Uniparental disomy (UPD) analysis
- Genomic knowledgebase
- Multiomics data analysis
- Pharmaceuticals
- Medical research
- Long-read sequencing compatibility
- Bioinformatics automation
- Long-read sequencing analysis
- Genomic data management
- Clinical variant filtering
- B2B
- NGS data interpretation
- Genomic discovery collaborations
- RNA sequencing integration
- Clinical genome research
- Genomic biomarker discovery
- Whole genome sequencing analysis
- Pharmacogenomics (PGx)
- Phenotype-driven variant prioritization
- Genomic variant detection
- PacBio analysis
- Multiomics integration
- Variant annotation and interpretation
- Star allele pharmacogenomics
- Structural variant calling
- Phenotypic evidence scoring
- Services
- Healthcare
- Oxford nanopore analysis
- Automated ACMG classification
- Automated workflow automation
- Genomics
- Genomic research tools
- Bioinformatics cloud solutions
- Data annotation and literature sources
- Data security and compliance
- Research and development in the physical, engineering, and life sciences
- Gene panel analysis
- Bioinformatics pipelines
- Bioinformatics pipeline customization
- Automated report generation
- Healthcare analytics
- Undiagnosed disease solutions
- Biotechnology
- Medical
- Health care
- Health, wellness & fitness
- Hospital & health care
Technologies Used
- AI
- MailJet
- Micro
- Microsoft Office 365
- Outlook
- Route 53
- Slack
- Zoho SalesIQ
