W14 – Computational challenges of third Generation DNA Sequencing data analysis

Workshop details

Date: Sunday September 4, 2016
Time: 9:00 – 17:00
Venue: World Forum, room: Central America

Organisers

Summary

The recent advances in technology and upcoming improvements in throughput of third-generation sequencing, e.g., from PacBio and Oxford Nanopore, open tremendous possibilities for the analysis of DNA or RNA molecules. However, many questions remain open for the field with respect to use in research and clinic. In particular, the type of data generated from these platforms poses significant challenging for computational analysis, because of the long read length and the relatively high error rate. New methods need to be devised to enable efficient read mapping, sequence assembly, variant calling and identification of modified bases.

To address the computational and technological opportunities and challenges that are coinciding with third-generation sequencing, we organize this workshop at ECCB on best practice of using these new sequencing platforms and their data analysis. These topics will be presented by a diverse panel of speakers who are highly familiar with either Nanopore or PacBio platforms. Representatives from the major commercial players in this field, i.e. Oxford Nanopore, Pacific Biosciences and BioNano Genomics were invited to join this meeting, so as to provide a broad view on the current technological levels and to give an outlook on future improvements and computational challenges that researchers may be faced with.

Target audience

Our target audience are wetlab researchers, bioinformaticians and computational biologists who are analyzing or interested in Oxford Nanopore and PacBio data.

 

Draft programme

time speaker – title
09:00-09:05 Hans Jansen (ZF-screens) – Welcome
09:05-09:35 Stuart Reid (ONT) – What’s in a squiggle?
09:35-10:05 David Stucki (PacBio) – Applications of SMRT sequencing
10:05-10:35 Kees-Jan Francoijs (BioNano) – Integration of Next Generation Mapping (NGM) data into NGS pipelines for high quality
Genome Assembly & Structural Variation discovery
10:35-11:00 Coffee/tea
11:00-11:30 Hans Jansen (ZF-screens) – An improved European eel genome
11:30-12:00 Wigard Kloosterman (UMC Utrecht) – Detecting structural variation in the human genome using nanopore sequencing
12:00-12:30 Matt Loose (Uni Nottingham) – Real-time selective sequencing on the MinION
12:30-13:30 Lunch break
13:30-14:00 Erwin Datema (Keygene) – ONT sequencing of a plant pathogen and beyond
14:00-14:30 Yahya Anvar (LUMC) – The value of SMRT sequencing in personalized medicine
14:30-15:00 Gabino Sanchez Perez (WUR) – Bridging the Gap Between Micro and Macro: Genomic and Structural Variation in the
Tomato Clade
15:00-15:30 Coffee/tea
15:30-16:00 Christiaan Henkel (Leiden University/Generade) – New possiblities in genome assembly
16:00-16:30 Serghei Mangul (UCLA) – HapIso: An Accurate Method for the Haplotype-Specific Isoforms Reconstruction from Long
Single-Molecule Reads
16:30-17:00 Wigard Kloosterman (UMC Utrecht) – Wrap-up