Ambry Genetics | Company Profile
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Department Breakdown
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Keywords & Focus Areas
Ambry Genetics
Overview
Ambry Genetics is a clinical genomics diagnostics company based in Aliso Viejo, California, founded in 1999. It specializes in translating genetic research into clinical tests for hereditary diseases, particularly cancer and rare conditions. As a Tempus Company, Ambry operates a 60,000-square-foot CLIA/CAP-certified lab, processing around 400,000 patient samples annually with high efficiency.
The company offers a range of services including hereditary cancer analysis, exome sequencing for rare diseases, and genetics software solutions for medical facilities. Ambry is recognized for innovative genetic testing, being the first to provide full gene sequencing of CFTR and hereditary cancer panels. Supporting healthcare providers and patients, Ambry delivers precise genetic insights that enable personalized medicine through molecular profiling and maintains a strong commitment to open science and patient care.
Basic Information
| Industry | research |
|---|---|
| Founded | 1999 |
| Revenue | $300M |
| Headquarters | 1 Enterprise, Aliso Viejo, CA 92656, United States |
| Languages | English |
| Parent Organization | Tempus AI |
| Alexa Ranking | 314282 |
Contact Details
- Phone: +1 949-900-5500
- Website: ambrygen.com
- LinkedIn: linkedin.com/company/ambry-genetics
Key Focus Areas & Initiatives
- Molecular diagnostic testing
- Clinical diagnostic exome
- Breast cancer genetics
- Hereditary cancer
- Cardio genetics
- Neuro genetics
- General genetics
- Family history questionnaire
- Pedigree drawing tool
- Risk assessment tool
- Biotechnology research
- Genetic counseling support
- Candidate gene discovery
- Cardiology
- Clinical utility
- Cardiology genetics
- Genetic variant discovery
- Peer-reviewed publications
- Translational genomics
- Medical genetics
- Genomics
- Neurogenomics
- High-throughput sequencing
- Biotechnology
- Clinical exome sequencing
- Telemedicine
- Hereditary cancer panels
- Cardiogenomics
- Genetic testing innovation
- Genetic data management
- Healthcare technology
- Genomic data sharing
- Genomic sequencing technology
- Genomic medicine
- Medical diagnostics
- Laboratory accreditation
- Customer service
- Genetic diagnostics
- Gene classification
- Genetic testing for rare diseases
- Genomic innovation
- Cost-effective genetic testing
- Genetic research collaborations
- Services
- Genetic testing accessibility
- DNA analysis
- Variant confirmation
- Clinical research partnerships
- B2B
- CLIA-licensed
- Patient for life program
- Genetic mutation detection
- Laboratory quality assurance
- Concurrent DNA/RNA testing
- Medical research
- Healthcare
- Genetic screening
- Rare disease testing
- Oncology genetics
- Clinical laboratory services
- Risk assessment
- Genetic variant interpretation tools
- Next-generation sequencing
- Genomic diagnostics
- Oncogenomics
- Genetic data interpretation
- Laboratory automation
- Family risk assessment
- CAP-accredited
- Family studies
- Personalized medicine
- Genetic testing
- Variant interpretation
- Precision medicine
- Reanalysis of genetic data
- RNA analysis
- Gene-disease relationships
- Genomic research in diverse populations
- Family history assessment
- Genetic variant reclassification
- Variant classification
- Clinical genetics
- Genomic research collaborations
- Diagnostic laboratory
- Gene discovery
- Molecular diagnostics
- Genomic data security
- Personalized healthcare
- Multi-omic testing
- Genetic research
- Medical and diagnostic laboratories
- Neurological genetics
- Clinical genomics
- Genomic data analysis
- Genetic testing accuracy
- Rare disease
- Neurological disorders
- Advanced genetic testing
- DNA testing
- RNA testing
- Exome sequencing
- Patient education
- Clinical interpretation
- Genome medical
- Genetic counseling
- Sanger confirmation
- Billing and insurance
- Health plan coverage
- Sample submissions
- Patient access
- Clinical research
- Pharmaceutical services
- Multioomic testing
- Interactive gene coverage tool
- Familial risk assessment
- Oncology testing
- Cost-effective testing
- Accurate results
- Genetic variant discoveries
- Healthcare partnerships
- Clinical education
- Genetic risk management
- Patient-centered care
- Genomic innovations
- Biobank collaborations
- Genetic disease detection
- Patient support programs
- Scientific collaborations
- Webinars and seminars
- Healthcare providers
- Digital health solutions
- Emerging genetic technologies
- Medical
- Health care information technology
- Health care
- Health, wellness & fitness
- Hospital & health care
- Medical & diagnostic laboratories
- Medical practice
Technologies Used
- AWS SDK for JavaScript
- Amazon AWS
- Amazon CloudFront
- Amazon Elastic Load Balancer
- Amazon SES
- Apache
- DoubleClick
- DoubleClick Conversion
- Facebook Custom Audiences
- Facebook Login (Connect)
- Facebook Widget
- Frame
- Google Dynamic Remarketing
- Google Tag Manager
- Hotjar
- Hubspot
- Jira
- LabWare LIMS
- Linkedin Marketing Solutions
- Microsoft Office
- Microsoft Office 365
- Mobile Friendly
- MySQL
- OpenSSL
- Outlook
- PHP
- React
- Remote
- Salesforce
- Slack
- Spring Boot
- Stripe
- Symfony
- Vimeo
- VueJS
- YouTube