Does the thought of using a new genomic software analysis tool seem daunting?
The effort of changing connections with each piece of genomic software, hardware and data source can be a complex and lengthy process to complete let alone optimise. Different APIs, web interfaces, data servers, cloud systems, scripts and command line interfaces and billing mechanisms across different genomic technologies and workflows, running on different versions with regular vendors updates, all creates overhead to manage.
Genomical does all the work for you, with pre-integrated genomic tools in a single platform so you can connect once and access many!
- ✅ Franklin by Qiagen
- ✅ Illumina Connected Insights (ICI)
- ✅ Emedgene
- ✅ Basespace Sequence Hub
- ✅ Geneyx
- ✅ Oxford Nanopore Technologies EPI2ME
- ✅ Sophia DDM
- ✅ Qiagen CLC workbench
- ✅ PanelApp Australia
- ✅ and the ability to run any Nextflow pipeline … with more tools in the works!
Every day we hear how labs spend months (even years) integrating a single tool. With Genomical, not only have we integrated multiple, but we’ve standardised how it’s done.
It feels a bit like magic, but it’s what we’ve spent years perfecting. Our proprietary genomic orchestration service handles even the most complex of data workflows and the largest of batches.
Keen to see it in action? Get in touch and we can show you how easy it is.
Connect once, Access many.
