In this open discussion webinar, DNA Genotek and Illumina discuss what’s trending in whole genome sequencing (WGS).
To fully benefit from the vast quantities of data from TCGA, tools for easy data visualisation and analysis must be developed for use of the non-computational scientist. Our panel of experts discuss TCGA data and the tools needed to make sense of it.
Comparison of Single Nucleotide Variants in Sequencing Data Produced by Illumina and Oxford Nanopore Technologies.
Come hear from David Grieg, Bioinformatician at Public Health England to learn more about the application of the MinION for the surveillance of Shiga toxin-producing Escherichia coli O157:H7.
Our panel of experts come together to discuss the benefits and drawbacks on the use of saliva DNA in genetic studies and how it’s currently being used to diminish biases in our databases and uncovering the role of epigenetics in psychiatric disorders.
Learn more about Edico Genome’s new DRAGEN Virtual Long-Read Detection (VLRD) Pipeline, that’s the first variant caller dedicated to SDs, and is designed to run with short sequence reads generated at moderate coverage.
A discussion of the technology that is in use today that allows Metabolon to carry out n of 1 studies that enable precision medicine, as well as future technology. Available on-demand.
Looking at applications for the MinION in new molecular approaches for the taxonomy characterization of microbial communities aiming resolution at species and strain level. Available on-demand.
Overcoming challenges of transferring large data to and from the Cloud, while achieving maximum data transfer efficiency, reliability, and security. Available on-demand.
We’ve talked to Manuel Corpas about his recent novel ‘Perfect DNA’, where he explores how reality would look like if we were ranked by our “genetic score”.
What did the recent study using the CRISPR gene editing technique actually entail, and what did we learn from it?
Watch: Scientists safely correct a disease-causing mutation in early stage human embryos with gene editing.