Genomics

Sequencing and interpretation, from whole genome sequencing to solid tumors, from RNA sequencing to liquid biopsy. Our proprietary pipelines offer precise sequencing and interpretation to research organizations and clinics worldwide.

Diagnostic

With over 3 million COVID-19 samples analyzed, 30 thousands whole genomes sequenced in our clinical lab, 500 thousands reports generated, we provide governments and clinics with effective end-to-end solutions for diagnostics at scale.

pharma

Our platform achieves a more effective, less risky, drug repurposing for genetic diseases by leveraging our whole genome database and a graph neural network approach to drug discovery.

Software

Our Immensa Genomic Interpretation Software offers more precise and faster analysis of complex genomic data, using machine learning and a continuous feedback loop from our database and the clinical lab.

ABOUT US

We deploy genomic applications that have an impact in people’s lives, turning healthcare data into solutions for patients and doctors, leveraging our database and machine learning algorithms.

Our genomic-data-driven approach to diagnostics and therapeutic development impacts research and clinical decisions, giving mission critical tools and reports for healthcare professionals.

Enabling genomic-driven prevention
Oncology: solid tumor and liquid biopsy solutions
3 million COVID-19 samples analyzed
ISO13485
Unparalleled experience with whole genome sequencing
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PLATFORM

Turning genomic data into patient solutions

Diagnostics

End-to-end solutions for rare diseases, oncology, infectious diseases and women’s health.

Pharma

GWAS-driven drug discovery platform for effective drug repurposing for complex pathways.

Sequencing

Next generation sequencing at scale, run on our proprietary software platform for customized sequencing services and premium turnaround time.

Software

Clinically validated, Immensa proprietary software using machine learning for the analysis and interpretation of genomic data at scale.

Lab Integration

Software fully integrated with the clinical lab, using real-time data and machine learning to drive effectiveness and standardization in the lab.

Database

Proprietary whole genome database with statistically significant datasets across different continents and disease areas.

INDIVIDUALS

Our services designed for your health.

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PARTNERS

Genomic Research Clients

NEWS

Research

Dante Labs achieves ISO 13485 certification for its Genomic Interpretation Software Immensa

Leveraging an 18 month long clinical validation study of 500,000 samples CAMBRIDGE, England–(BUSINESS WIRE)–Dante Labs, a world leader in genomic sequencing and data analysis, announced today that it received ISO 13485:2016 certification for its Immensa Genomic Interpretation Software as a medical device. The highly coveted industry certification involved a deep clinical validation study carried out …

Corporate

Dante Labs appoints Illumina acclaimed COO Bob Ragusa as Board Member to support the execution of its global integrated precision medicine strategy

July 19, 2021 07:07 ET Bob Ragusa leads Illumina global operations and is a key contributor to Illumina’s growth and global scaling.Dante Labs integrated precision medicine offering leverages the intersection of local lab operations with centralised software and database.Dante Labs mission is to accelerate science to patients to save more lives. CAMBRIDGE, United Kingdom, July …

Genetics

The Genetics of Cystic Fibrosis

Genetic testing for Cystic Fibrosis can make the difference What is Cystic Fibrosis Cystic Fibrosis is a genetic disease that mainly affects the lungs and digestive system, but it can result in fatal complications such as liver disease and diabetes. The defective gene responsible for Cystic Fibrosis leads to the creation of thicker, stickier mucus …

A new approach to your health.

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