Advance your research. Understand NGS and analyze sequenced data yourself.
December 8-10, 2021
9 am - 5 pm (CET UTC+1)
The purpose of this workshop is to get a deeper understanding in Next-Generation Sequencing (NGS) with a special focus on bioinformatics issues. Advantages and disadvantages of current sequencing technologies and their implications on data analysis will be discovered. The participants will be trained on understanding their own NGS data, finding potential problems/errors therein and finally perform their first downstream analysis (variant calling). In the course we will use a real-life NGS dataset from the current market leader illumina.
All workshop attendees will be enabled to perform important first tasks of NGS data analysis themselves. The course layout has been adapted to the needs of beginners in the field of NGS bioinformatics and allows scientists with no or little background in computer science to get a first hands-on experience in this fast evolving research topic.
The online course will make use of a web conferencing system. Hands-on NGS analysis will be performed in an interactive browser-based data analysis platform. Before the course, you will get a printed manuscript.
Our trainers have a proven record of academic and/or industrial experience in NGS data analysis. Because up-to-date expert knowledge is needed to answer your questions and know what is important in the field.
We only use open source tools that are free to use. We try to showcase and compare different tools (e.g. NGS mappers), since not every software fits with every task/question.
For a optimal learning experience we carefully prepare our learning materials and example data.
This workshop has been adapted to the needs of beginners in the field of NGS bioinformatics and comprises this three course modules:
Dr. David Langenberger (ecSeq Bioinformatics GmbH)
David started working with small non-coding RNAs in 2006. Since 2009 he uses NGS technologies to investigate these short regulatory RNAs as well as other targets. He has been part of several large NGS projects, for example the International Cancer Genome Consortium (ICGC).
Dr. Mario Fasold (ecSeq Bioinformatics GmbH)
Mario works in the analysis of microarray data since 2007 and developed several bioinformatics tools such as the Bioconductor package AffyRNADegradation and the Larpack program package. Since 2011 he specialized in the field of NGS data analysis and helped analysing sequencing data of several large consortium projects.
The target audience is biologists or data analysts with no or little experience in analyzing NGS data. A fundamental understanding of molecular biology (DNA, RNA, gene expression, PCR, ...) is assumed.
A basic knowledge of Linux & Bioinformatics (commandline usage, common commands and tools) is not required.
A current desktop computer / laptop with an up-to-date browser (Firefox or Chrome) is required.
Available Seats: 25 (first-come, first-served)
Registration Fee: 789 EUR (excluding VAT)
Opening Date of Registration: May 1, 2020
Closing Date of Registration: December 1, 2021
Workshop: December 8 - 10, 2021 from 9 am to 5 pm (CET UTC+1)
Find out what time it is at your location: Time Difference
"Surprisingly I got sucked into the topic, which I thought would be very boring. I have the feeling I learned a lot and can understand the sequencing process much better. Thank you!" Elisabeth M., LK Mistelbach, Germany
"It is a very condensed course, covering really practical tricks for beginners on coding in Linux, and basically all the primary steps dealing with NGS data. Really worths the contribution of the fee and the time spent :)" Tianhao Zhao, University of Groningen, Netherlands
"It was a good and easy to follow introduction into the topic and even though I had some prior experience with some of the tool presented it filled some knowledge gabs and will improve my work in the future." Dr. Michael Helmut Hagemann, University of Hohenheim, Germany
When you register for this workshop you are agreeing with our Workshop Terms and Conditions. Please read them before you register.
What you need:
The course cannot be run on phones, tablets and similar handheld devices.
We will start every morning at 9am sharp and work together until 5pm in the afternoon. There will be regular short breaks and a longer break at lunchtime.
As this is a live broadcast, you cannot pause the course and continue later. The individual exercises build on each other, so you should not leave in between.
No, you do not have to install any software to follow the course. You will get access to a high performance computer in the cloud, which you can easily log into using an in-browser console. All necessary programs are already installed on this computer. This way, we can start right away.
Of course we'll help you. If such a case should occur, we have assistants in the virtual room whom you can contact via chat. They can discuss your issue in a separate room/chat. They can also dial into your in-browser console and see exactly the same as what you see. This way they can help you directly and without much detour.
Note: The assistent can only see your in-browser terminal window but nothing else and also do not have any access to your computer.
A few days before the course we will send you the manuscript by mail. After the course, you will receive a download link for our Live-Linux system with pre-installed NGS tools. When you start this with a virtualization tool (such as the free VirtualBox), a live version of Linux will be running on your computer where you can repeat and/or practice all the tasks of the course.
We have tried to keep the differences between the online and the attendance courses as small as possible.
Before the event: If you like to travel and get to know new cities, you will miss that in an online course. But, with an online workshop, you will obviously have to organise and plan much less. Travel and accommodation are not necessary. Likewise, you will not have any lost days of arrival and departure.
During the event: The possibilities for networking (e.g. during the conference dinner) are unfortunately very limited. But of course we will try to answer your questions online as well. There will be a Q&A moderator to whom you can write your question anytime. The moderator will then decide if your question should be answered directly or in a Q&A session at the end of each chapter.
ecSeq Bioinformatics GmbH