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biomodal is an omics-based life sciences technology and analytics company delivering products that bring the dynamism of our ever-changing biology into focus. Our duet multiomics solution enables more epigenetic information from a single, low input DNA library without complex, resource intensive bioinformatics or harsh chemical treatment. Our single-base-resolution, phased sequencing approach unlocks the combinatorial power of genetic and epigenetic information in one workflow, elucidating greater biological insight within the fields of cancer, neurodegenerative disease, and ageing.
One sample, one workflow, one solution for multiomic insights
duet multiomics solution +modC simultaneously sequences genetics & epigenetics in a single workflow. See all four genetic bases (A-C-G-T) without ambiguity in C or T calls – plus modified cytosine (modC) using your existing next-generation sequencer, with results phased within a single read.
Product Features:
Whole Genome Investigation: Get simultaneous whole genome sequencing results with standard SNP detection and epigenetic marks with improved sensitivity and specificity.
Preserve Valuable Samples: Utilize samples as low as 10 ng of DNA for highly accurate modC.
C-to-T Mutation Detection: Simultaneously detect the most common type of genetic mutation (C-to-T) in the human genome and cancer.
Allele-specific methylation: Attain phased results for allele-specific methylation (ASM) without loss of even gen
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