Next Generation Sequencing (NGS) bioinformatics resources are being widely implemented in NGS panel and NGS Exome sequencing in clinical genetic testing. Our NGS bioinformatics workshop & symposium is designed for medical genetic testing and services laboratories that look for rare mutations in human patient samples using NGS technologies, platforms and software. Both national health service genetic labs and private companies will benefit from this event by learning how leading laboratories are tackling the analysis and interpretation of NGS sequence data.
The aim of this event is to cover various aspects of NGS bioinformatics in a clinical setup, from general theoretical aspects to more specific “hands-on” approach. For this reason this 2-day event will comprise a symposium & a workshop, to give the participant a good in-depth view of NGS bioinformatics and latest developments from labs and software companies.