Lab automation for cancer genomics
Lab automation for cancer genomics
Despite the advances in next-generation sequencing, opportunities remain to better utilise genomic capabilities for cancer detection, characterisation, and monitoring.
This webinar will cover the latest in robust sequencing of cancers in the clinics, and how we can scale up our capabilities to better support patients going forward.
Improving accuracy and consistency of variant interpretation for cancer susceptibility genes – Alice Garrett, Clinical Research Fellow, Institute of Cancer Research
Lab automation for cancer genomics – Craig Johnston, Diagnostics & Genomics Lead, Automata
Integrating whole genome sequencing into clinical practice for cancer patients – Alona Sosinsky, Scientific Director of Cancer, Genomics England.
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Watch Francis Crick Institute’s Jérôme Nicod discusses the impact of automating genomic workflows including Amplicon library preparation, FFPE RNA extraction, and COVID-19 sequencing.
Watch Francis Crick Institute’s Jérôme Nicod discusses the impact of automating genomic workflows including Amplicon library preparation, FFPE RNA extraction, and COVID-19 sequencing.
In this webinar Russell Green, Automata’s Director of Product Growth, talks about how reshaping cell biology experiments for automation will enable labs to overcome common challenges