Unlocking Genomic Discoveries: Seamless Access to the Sequence Read Archive
Read more
Blog
On April 29, 2025 | By Zelia Worman
Medicine moves
too slow
At Velsera, we’re changing that.
Velsera in a nutshell
Velsera is a Health Tech company
providing advanced software enabled by expert services
that accelerates the discovery, development and delivery
of Precision Medicine globally.
We are on a mission to make breakthroughs happen faster,
so that lives are improved sooner.
Who we serve
Velsera accelerates clinical & discovery breakthroughs.
Biotech &
Pharma
Accelerate your research breakgthroughs and novel drug launches.
Clinical Diagnostic Labs
Accelerate the scale up of your genetic testing & unlock the value in your data.
NGS Assay & Equipment Manufacturers
Bring new tests to market and scale up testing fast.
Non-Profits and Government Agencies
Accelerate your research breakthroughs and unlock the value in your data.
Velsera is uniquely able to accelerate across the gap between Clinical & Discovery.
Velsera pushes medicine forward
As one of the largest omics analytics providers in the market
80+
Active clinical NGS lab customers
250,000+
NGS samples sequences
20+
Productized NGS assays available 'off the shelf'
+20% p.a.
Year over year sequencing volume
Advancing breakthrough discoveries to tackle the world's most pressing health challenges
7/10
Top pharmas supported by our technology-enabled products and services
18,000+
Researchers using the Seven Bridges Platform
1.7 Million
Patients
48 PB
Of multi-omic molecular data
Trusted widely across the industry
A selection of our customers
Velsera solves problems by combining deep expertise with cutting edge tech
Powerful platforms
One singular vision
Technology designed to accelerate the momentum of medicine
Seven Bridges
Our Trusted Research Environment (TRE) for bioinformatic analysis & pipeline development.
GRAF
Our award winning reference genome tool.
ARIA
Our data harmonization and secure sharing platform.
Clinical Genomics Workspace
Our tertiary analytics & reporting tool for clinical NGS diagnostics.
Knowledgebase
Our best in class, IVD-grade variant interpretation knowledge base.
Expert services
Unified for impact
Services crafted to drive transformative advancements in healthcare
Data Harmonization
Supporting health & life science companies to combine and harmonize their data.
Bioinformatics
Supporting researchers and diagnostic developers to build better workflows
Scientific
Supporting researchers to run efficient and effective studies.
Regulatory
Supporting clinical diagnostic labs and diagnostic test developers to navigate the changing regulatory environment.
Clinical
Supporting diagnostic labs to start and scale-up their NGS testing.
Our Integrated Solutions ‘menu’.
Clinical & Multi-omic Data Access
Harmonize and augment your data to unlock the value within.
Analysis & Bioinformatics
Use cutting edge technology to make new discoveries and breakthroughs faster.
Companion Diagnostic Development & Scaling
Develop better diagnostics that scale faster, accelerating novel drug uptake.
NGS Assay Development & Expansion
Bring new tests to market and scale-up fast.
IVD Compliance Transition
Effectively navigate and grow in the changing regulatory environment.
Clinical Interpretation & Reporting
Accelerate the scale up of your genetic testing & unlock the value in your data.
Testimonials
Hear how leading life sciences companies and clinical diagnostic labs trust our technology to accelerate discovery and improve patient care.
Blog
Latest Posts
Blog
On April 2, 2025 | By Zelia Worman
The Role of AI and LLMs in Accelerating Precision Medicine
Read more
Blog
On April 14, 2025 | By Laura Buttrum
In Vitro Diagnostic (IVD) Assays: the Promises and Pitfalls of Standing up new NGS Testing
Read more
Blog
On December 3, 2024 | By Julie Furt
Community is the Key to Progress with Precision Medicine
Read more