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Introduction to Bioinformatics using NGS data, 2 hp (location: Göteborg)


Kursnummer50,6
År2017
TypMethodcourse
Spår-
Max antal deltagare30
Sista ansökningsdag2016-04-05
SpråkEn
KursansvarigManfred Grabherr
InstitutionSciLifeLab, and Bioinformatics Core Facility at the University of Gothenburg.
BesöksadressMedicinaregatan 3, Göteborg
Postadress
Datum2017-05-15 to 2017-05-19
LokalMedicinaregatan 3, Göteborg
Kurslängd5 days
Kursrapport 
Kursplan 

 

Beskrivning

The course will provide an entry-level introduction to a wide range of analytical techniques for massively parallel sequencing, including basic Linux commands. We will pair lectures on the theory of analysis algorithms with practical computational exercises demonstrating the use of common tools for analyzing data from each of several common sequencing study designs.

Inlärningsmål

Learn analytical techniques for massively parallel sequencing, and how to apply them to your own research project.

Innehåll

Topics covered will include:

Basic Linux usage
NGS read-to-reference alignment (genomic and RNA-Seq)
Variant calling in populations
De novo assembly of RNA-sequence data
Reference-guided RNA-Seq expression analysis
Data management

Undervisning

Applicants are only accepted via the course webpage:
https://www.scilifelab.se/events/ngsdatagbgvt17/

Course location: Göteborg

Course fee: 1800 SEK.

Examination

Participation on all lectures, exercises and discussions.

Litteratur

Will be provided during the course

Lärare

Manfred Grabherr, Magnus Alm Rosenblad

Kontakt

https://www.scilifelab.se/events/ngsdatagbgvt17/

education@scilifelab.uu.se

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