Finally see it all
Uncover the biomarkers you’re searching for with a single workflow solution. biomodal’s multiomic analysis provides both genetic and epigenetic data simultaneously with groundbreaking clarity, precision and speed.
One sample, one workflow, one solution
duet multiomics solution +modC workflow
This approach provides the most efficient way to obtain genetic and methylation information simultaneously.
Conventional methods: 2 samples, 2 workflows, 3+ data analyses
These approaches require splitting the sample and running parallel workflows, with multiple data analyses and significant information loss.
A single comprehensive workflow to uncover the DNA modifications that matter
Applications for multiomics discovery
Cancer research
Multiomics analysis offers a deeper understanding of the drivers of cancer. Our technology allows you to bring multiomic analysis to your research using your existing DNA sequencing infrastructure.
Ageing
Probe and determine the markers of biological age to better understand age-related diseases including Alzheimer’s disease, osteoporosis, type II diabetes and chronic heart disease.
Population genetics
Investigate genome-wide methylation patterns across populations with a single solution and integrated data.
Non-invasive prenatal testing
Combining genetic and epigenetic DNA sequencing has the potential to reduce the time taken to detect pregnancy complications and significant genetic and epigenetic variations in a foetus.
Neurodegenerative disease
Reveal the role of DNA methylation in the most common neurodegenerative diseases, and identify potential targets for promising therapeutics.
Precision medicine
Use multiomics analysis to identify targets for promising therapeutics tailored to the genetics and epigenetics of the individual.