ARANGS13 Automated and reproducible analysis of NGS dataDownloadable poster in PDF |
IMPORTANT DATES for ARANGS13
Deadline for applications: October 8th 2013 Notification of acceptance dates: October 15th 2013 Course date: October 21st - October 24th 2013 |
Instructors: |
Rutger Vos studied biology at the University of Amsterdam, where he graduated in
2000. He then embarked on his PhD research under professor Arne Mooers at Simon
Fraser University in Vancouver, Canada, where he defended his thesis on
phyloinformatic problems in 2006. As a self-taught programmer he then became
involved in several open-source scientific software development projects while
continuing his research career through a postdoctoral fellowship at the
University of British Columbia (Vancouver, Canada) and a Marie Curie research
fellowship at the University of Reading (Reading, UK). In Spring of 2012 he
commenced his employment as the bioinformaticist of the Naturalis Biodiversity
Center in a role where he combines novel research with
bioinformatics contributions to various research programmes within the
organization. In his spare time he also contributes to various open source
software projects (TreeBASE, Bio::Phylo, NeXML) and is co-PI of the
PhyloTastic project. In addition Rutger has taught bioinformatics workshops in
the US, Japan, China, Kenya and twice before at GTPB
(PHYLOINF09) and
ARANGS12).
|
Darin London studied biology at Texas Tech University in the
United States, graduating with a Masters of Science in 1999. He has been
supporting biological research with computational support for 12 years, starting
at GlaxoSmithKline in 2000, then moving to the European Bioinformatics Institute
to work on the Biomart system, and finally coming to the Institute for Genome
Sciences and Policy at Duke University, Durham, USA in 2005. He has developed
automated analysis pipelines to help researchers analyze over 25Tb of Vertebrate
NGS data (GAII and HiSeq), mostly involving research work on the Encyclopedia of
DNA Elements (ENCode). Darin has taught numerous workshops on programming and
automation with the Perl programming language, including the phyloinformatics
workshops at the NESCent, Durham, USA, and the GTPB
(PHYLOINF09) and
ARANGS12). |
Course DescriptionIntroductionNext generation sequencing (NGS) technologies for DNA have resulted in a yet bigger deluge of data. Researchers are learning that analysing such data sets is becoming the bottleneck in their work. In many cases, several steps in these analyses are fairly generic (e.g. quality control filtering, alignment to reference sequences, typing) so that off-the-shelf pipelines can be applied. In other cases, novel research approaches require development of new analysis pipelines. Either way, all analysis steps should be repeatable and any changes made to the data (e.g. renaming, annotation, alignment) should be recorded so that the provenance of the results is clear and inferences are reproducible. In this brief workshop we will establish several best practices of reproducibility and provenance recording in the (comparative) analysis of data obtained by NGS. In doing so we will encounter the commonly used technologies that enable these best practices by working through use cases that illustrate the underlying principles. Building on the basis of workflow development, we will further illustrate how custom-built workflows can be manipulated using graphical platforms (e.g. Galaxy, Taverna, etc.).Best practices
Technologies
Use cases
Target audienceThis course is aimed at researchers who've recently embarked on NGS projects and now, faced with large amounts of data, would like to learn how to automate generic analysis steps and develop new ones in a reproducible (and shareable) way. The course will be illustrated with examples from specific single-celled and multicellular taxa but the concepts are applicable to any species not explicitly referred to in the course. The ideal attendee is a scientist who is not afraid to get his/her hands dirty to acquire the computer-literacy skills for dealing with the informatics side of data analysis.Pre-requisitesThe course assumes that attendees are not intimidated by the prospect of gaining experience working on UNIX-like operating systems (including the shell, and shell scripting) as well as interpreted programming languages (e.g. R, Perl, Python). Attendees should understand some of the science behind high-throughput DNA sequencing and sequence analysis, as we will not go deeply into underlying theory (or the mechanics of given algorithms, for example) as such. What will be taught are technical solutions for automating and scaling up such analyses, which will include (but is not limited to) beginner-level programming. General computer literacy, (e.g. editing plain text data files, navigating the command line) will be assumed. |
Detailed Program |
Instituto Gulbenkian de Ciência, Apartado 14, 2781-901 Oeiras, Portugal Last updated: October 1st 2013 |