Genomics
Whole-genome and whole-exome sequencing, variant analysis and related short- and long-read workflows.
- Illumina, PacBio and ONT
- Variant calling and annotation
- Population-scale workflows
These categories describe the analyses that can run within an Invitromics environment. Final tools and resources are selected during project scoping.

Whole-genome and whole-exome sequencing, variant analysis and related short- and long-read workflows.
Bulk, single-cell, single-nucleus and spatial transcriptomic workflows.
Proteomics, metabolomics, epigenomics, metagenomics and integrative analysis.
Reproducible predictive modelling and data-driven discovery for complex biomedical datasets.
Research pipelines, APIs, databases and analytical applications.