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Illumina NGS Applications: RNA-Seq and DNA sequencing for genetic disease How can RNA sequencing help you measure gene expression, identify new isoforms, transcripts, and fusion genes? In this seminar we will show you how to answer these questions and more. From experimental design through to data analysis, explore the latest solutions for studying the transcriptome. You'll learn how RNA-Seq offers: Higher quality data, simple workflows and better value Discover how new technologies are being used to identify genetic variations associated with human disease. In the afternoon session you’ll learn how high-throughput genetics is expanding the field of human disease research. You'll learn about: Whole genome sequencing and array-based discovery is advancing research in multiple areas Exome studies are scaling beyond mendelian disease and targeted panels are being effectively used to identify statistical associations Monday, March 12, 2012 Guy’s Tower - Medical and Molecular Genetics Department Seminar Room, Floor 8 St Thomas Street, London, SE1 9RT SEMINAR SCHEDULE 11.00 Registration 11.30 Introduction 11.45 RNA-Seq, what is it and how should I design my experiment? 12.15 RNA-Seq, sample preparation through to data analysis, considerations and best practices 12:45 Lunch 14.15 Whole genome sequencing 14:45 Targeted resequencing 15.15 Seminar Closes Register now: www.illumina.com/events/seminars/illumina_eu_seminars.ilmn