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Duet multiomics solution with evoC workflow and software for efficient NGS integration and large-scale multimodal data analysis.
Credit: Biomodal

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Duet multiomics solution evoC

Duet multiomics solution evoC
Credit: Biomodal

One sample, one workflow, one solution.

 

Duet multiomics solution evoC is comprised of a pre-sequencing workflow requiring as little as 10ng gDNA or 5ng cfDNA that seamlessly integrates with NGS sequencing platforms and a post-sequencing software package to accelerate data analysis. The post-sequencing software trims, aligns, and annotates to generate analysis-ready BAM, VCF, BedMethyl, and ASM files. Additional plugins include proprietary analysis software that facilitates analysis of multimodal data at scale.


 Multimodal explorations enabled by the 6-base genome: 

  • Understand the interplay between genetics and epigenetics 
  • Explore how methylation and hydroxymethylation differ between healthy and disease
  • Understand the mechanisms of epigenetic gene regulation 
  • Discover more sensitive multimodal biomarkers for disease
  • Build more accurate multimodal disease classifiers 
  • Detect biological change or disease earlier
  • Explore gene expression and chromatin architecture in otherwise inaccessible samples such as FFPE and cfDNA 
  • Use gene regulatory elements to understand the biological trajectory of your sample

Product Specifications
Input requirements cfDNA 5-30ng gDNA 10-80ng
Assay time Approx. 18 hours
Assay hands-on time Approx. 10 hours
Shelf-Life Minimum 3 months
Resolved FASTQ Unaligned 6-base data
6-base BAM Aligned 6-base data for downstream analysis
VCF file Germline variant calls
QC reports csv and html reports
Zarr store 6-base methylation analysis
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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