Schedule
Section outline
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Thursday 08 November 2018 Mini-symposium
Introduction 09:00 Introduction to the current technologies used for long read sequencing - Andrea Patrignani (ETHZ and SIB) 09:45 Reference-based gene expression analysis with long-read sequencing data - Charlotte Soneson (University of Zurich, FMI and SIB) 10:10 Coffee break 10:30 Improving protein-coding gene calls using a long-reads based genome assembly - Amina Echchiki (University of Lausanne and SIB) 10:55 Applications of single molecule sequencing: alternative splicing, rare variants and methylation - Giancarlo Russo (ETHZ and SIB) 11:20 Integrating NGS data for the assembly of prokaryotic genomes & a proteogenomics approach to identify their complete protein-coding potential - Christian Ahrens (Agroscope and SIB) 11:45 Studying Bacterial gene flow in real time; The benefits of using long reads data - Marc Garcia Garcera (University of Lausanne and SIB) 12:10 Round table with the speakers 13:00 Lunch End of the minisymposium
Hands-on 14:00-17:30 Hands on - Amina Echchiki (University of Lausanne and SIB) and Walid Gharib (University of Bern and SIB)
In this session, the participants will familiarise with the raw long reads, learn how to assemble genomic reads, how to map genomic and RNA-seq reads to a reference genome, and finally how to proceed to transcriptome assembly.
Friday 09 November 2018 Hands on 09:00 - 12:30 Hands on - Amina Echchiki (University of Lausanne and SIB) and Walid Gharib (University of Bern and SIB)
In this session, participants will interpret assemblies they have computed on the first day, learning how to assess quality of a genome assembley and run dowstream analysis.
12:30 Lunch Hands on 14:00 - 17:30 Analysis of PacBio Long Reads using the SMRT Analysis Package and SUSHI - Weihong Qi and Giancarlo Russo (ETHZ/SIB)
This session consists of lectures providing an overview of the individual pipelines in the SMRT Analysis Package as well as hands-on exercises using the SUSHI data analysis framework developed at FGCZ, including quality control of PacBio data and data preparation, sequence alignment and variant detection, de novo assembly.