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Next-Generation Sequencing Data Analysis: A Practical Introduction Quality Control, Read Mapping, Visualization and DNA Variant Analysis In a Nutshell Learn the essential computing skills for NGS bioinformatics Understand NGS technology, algorithms and data formats Use bioinformatics tools for handling sequencing data • Perform first downstream analyses and call variants Scope and Topics 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 se- quencing 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 (DNA variant calling). In the course we will use a real-life RNA-seq dataset from the current market leader illumina. All workshop attendees will be enabled to perform important first tasks of NGS data analysis them- selves. The course layout has been adapted to the needs of beginners in the field of NGS bioinfor- matics and allows scientists with no or little background in computer science to get a first hands-on experience in this new and fast evolving research topic. Trainers Dr. David Langenberger Dr. Mario Fasold ecSeq Bioinformatics GmbH ecSeq Bioinformatics GmbH Registration Fee 949 EUR (excluding VAT) DATE March 25 - 27, 2020 TIME 9 am – 5 pm VENUE Munich, Germany Advance your research. Understand NGS and analyze sequenced data yourself. The target audience is biologists or data analysts with no or little experience in analyzing NGS data. Included in the Course Course materials Catering during the workshop Conference dinner High-performance workstations (no laptop needed) USB-Stick for taking home results and analysis ecSeq Bioinformatics GmbH · Sternwartenstr. 29 · 04103 Leipzig · Germany twitter.com/ecSeq· [email protected] · www.ecseq.com Enroll Today! ecseq.com/workshops/public

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Next-Generation Sequencing Data Analysis: A Practical IntroductionQuality Control, Read Mapping, Visualization and DNA Variant Analysis

In a Nutshell• Learn the essential computing skills for NGS bioinformatics• Understand NGS technology, algorithms and data formats• Use bioinformatics tools for handling sequencing data• Perform fi rst downstream analyses and call variants

Scope and TopicsThe 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 se-quencing technologies and their implications on data analysis will be discovered. The participants will be trained on understanding their own NGS data, fi nding potential problems/errors therein and fi nally perform their fi rst downstream analysis (DNA variant calling). In the course we will use a real-life RNA-seq dataset from the current market leader illumina.

All workshop attendees will be enabled to perform important fi rst tasks of NGS data analysis them-selves. The course layout has been adapted to the needs of beginners in the fi eld of NGS bioinfor-matics and allows scientists with no or little background in computer science to get a fi rst hands-on experience in this new and fast evolving research topic.

Trainers

Dr. David Langenberger Dr. Mario Fasold ecSeq Bioinformatics GmbH ecSeq Bioinformatics GmbH

Registration Fee949 EUR (excluding VAT)

DATE March 25 - 27, 2020 TIME 9 am – 5 pm VENUE Munich, Germany

Advance your research. Understand NGS and analyze sequenced data yourself.The target audience is biologists or data analysts with no or little experience in analyzing NGS data.

Included in the Course� Course materials� Catering during the workshop� Conference dinner� High-performance workstations

(no laptop needed)� USB-Stick for taking home results

and analysis

ecSeq Bioinformatics GmbH · Sternwartenstr. 29 · 04103 Leipzig · Germanytwitter.com/ecSeq· [email protected] · www.ecseq.com

Enroll Today!

ecseq.com/workshops/public