Short-read analysis
Processing of panel, exome and whole-genome sequencing data, with variant filtering, interpretation and reporting.
Find the solution
that fits your needs.
Choose analysis and reporting, an institutional computing system, longevity laboratory services or training. We define the scope around your samples, data and intended use.
Analysis & reporting
You have sequencing data and need processing, interpretation and reporting.
Gennext for short-read and long-read data.On-site hardware
You want analyses to run within your institution’s infrastructure.
Worker Nodes configured for your workload.Longevity laboratory
You need laboratory work for genetic and epigenetic assessment.
Microarray and Nanopore long-read sequencing.Practical training
You want to develop skills in variant assessment and platform use.
Medical genomics courses and video resources.01 / GENNEXT
Sequencing data.
Findings you can assess.
We analyse short-read and long-read sequencing data, from quality control and variant assessment to reporting. Gennext Clinical supports somatic and germline workflows; Gennext Longevity brings genetic and epigenetic findings into professional wellness services.
Longevity reports support personalised health guidance; they are not diagnostic tests.
02 / WORKER NODE
Your analysis infrastructure.
At your institution.
A Worker Node is a computing unit that runs genomic analysis tasks on site. Capacity and deployment are planned around data volume, concurrent analysis needs and your existing infrastructure.
- Capacity planned for sample volume and concurrent workloads
- Coordinated computing and storage planning
- Deployment suited to existing infrastructure
Worker Node
On-site analysis workstation
High-throughput server
For intensive and concurrent analysis workloads
GENNEXTOne platform. Distributed analysis.
Central coordination
User access · Task assignment · Workflow status
Analysis tasks and status information
Institution A
LOCAL INFRASTRUCTURE
Genomic data→Worker Node→Analysis output
Data and computing stay on site
Institution B
LOCAL INFRASTRUCTURE
Genomic data→Worker Node→Analysis output
Data and computing stay on site
Institution C
LOCAL INFRASTRUCTURE
Genomic data→Worker Node→Analysis output
Data and computing stay on site
Access, task and workflow metadata required for coordination are shared with central services.
Local processing, central coordination
Genomic inputs and analysis outputs are processed on the assigned local infrastructure. Central services coordinate user access and analysis tasks.
LONGEVITY LABORATORY
From the laboratory
to personal health insights.
Our laboratory performs microarray and long-read sequencing work, supporting genetic and epigenetic assessment within our longevity services.
MICROARRAY
Genetic and epigenetic profiling
Genotyping and DNA methylation workflows provide data for genetic predisposition and epigenetic assessment.
LONG-READ
Long-read sequencing
We sequence long DNA fragments with Nanopore technology and analyse the resulting data for the aims of each study.
04 / Training
Medical genomics training
Our medical genomics training addresses variant interpretation and prioritisation. Contact us for programme scope and participation details.
Germline variants
- Variant evaluation in inherited disorders
- Considering phenotypes alongside genetic findings
- Approaches to variant prioritisation
Somatic variants
- Evaluating genomic findings in oncology
- Variant filtering and evidence review
- Preparing findings for reporting
GENNEXT
Get to know Gennext.
Discover the platform in our introduction video. Visit Gennext Community for tutorials and analysis workflows.
Let’s find the right solution for your organisation.
Talk to us about your software, infrastructure and training needs.