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Duet Multiomics Solution evoC

Duet Multiomics Solution evoC
Credit: Biomodal


Reveal the power of the 6-base genome with duet multiomics solution evoC. The combinatorial genetic and epigenetic technology provides single-base-resolution sequencing data that reveals standard four-base sequencing (A, G, C, and T), and distinguishes between 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC), on the same DNA molecule. This added resolution will allow greater power in detecting disease associations, identifying novel biomarkers, developing disease classifiers, and monitoring the progression of disease; even with limited samples such as cell-free DNA (cfDNA).  


The advanced 6-base genome data enables the exploration of epigenetic mechanisms of gene regulation through methylation and hydroxymethylation. Researchers now are able to obtain an accurate measurement of 5mC and 5hmC, integrated into local genetic context, with >95% of bases above Q30 and 50% with accuracy above Q40. By measuring multiple modes of biology from a single low-input DNA sample in a single experiment, researchers can use the comprehensive data to build predictive models of gene expression, chromatin accessibility, and enhancer status to better understand the biological mechanisms that link genotype to phenotype. 



Product Specifications
Input Requirements cfDNA: 5-50ng gDNA: 10-80ng
Environment Commercial cloud On site HPC
Installation time Commercial cloud: Fast On site HPC: dependent on institution
User interface Command line interface
Output files QC reports, BAM, BedMethyl, VCF, Quant, ASM
Assay time Approximately 18 working hours
Assay hands-on time Approximately 10 hours
Shelf-life Minimum 3 months
About biomodal
biomodal is focused on building technologies as research tools for life scientists and clinical developers. Their technology allows you to capture the 6-base genome and provide insight into the complexity and dynamism of cellular interactions. biomodal's platform works with your existing infrastructure, integrating a pre-sequencing workflow with post-sequencing informatics to generate highly accurate genetic and epigenetic data from a single sample in a single run.
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