The leading conference on human genetics in Europe.
Associate Director, Customer Collaborations
biomodal
Dive deeper into how acquiring genetic and methylation data simultaneously produces higher quality calls that show how methylation promotes or silences specific alleles causing deregulation, altered expression, or potential disease.
Senior Bioinformatics Scientist
biomodal
Review performance of duet multiomics solution +modC for the detection of genetic and epigenetic sequence data at base resolution when using formalin damaged DNA. Samples include formalin-compromised DNA standards (fcDNA) as well as DNA extracted from formalin-fixed and paraffin-embedded (FFPE) samples of two colorectal cancer (CRC) patients.
Here are the relevant biomodal resources for information. Find poster presentation information, case studies, interviews, and more.
Gain complete genetic and epigenetic methylation information from your DNA library in a single workflow. All four genetic bases (A-C-G-T) without ambiguity in C or T calls – plus modified cytosine (modC) using your existing next-generation sequencing pipeline, phased within a single read.
The Aparicio lab at the British Columbia Cancer Research Centre (BCCRC) utilises 5-letter sequencing technology, duet multiomics solution +modC, to investigate ‘epigenetic rewiring’ in breast cancer cells.
Learn how simultaneous measurement of genetics and epigenetics with duet multiomics solution +modC enables the study of allele-specific methylation and how this can be used to understand the impact of epigenetic rejuvenation.
Review performance of duet multiomics solution +modC for the detection of genetic and epigenetic sequence data at base resolution when using formalin damaged DNA. Samples include formalin-compromised DNA standards (fcDNA) as well as DNA extracted from formalin-fixed and paraffin-embedded (FFPE) samples of two colorectal cancer (CRC) patients.
