Bioinformatics: Whole Exome Sequencing and RNA-sequence data analysis
This course covers state-of-the-art tools and methods for NGS RNA-seq and exome variant data analysis, which are of major relevance in today's genomic and gene expression studies. Further information is available here.
Please note that if you are not eligible for a University of Cambridge Raven account you will need to book by linking here.
The course is oriented to experimental researchers, post-doctoral and PhD students who want to learn about the state-of-the-art of genomic variant and transcriptomics data analysis methodologies and carry out their own analysis.
Basic computing skills and graduate level in Life Sciences.
Number of sessions: 3
# | Date | Time | Venue | Trainers | |
---|---|---|---|---|---|
1 | Mon 29 Sep 2014 09:30 - 17:30 | 09:30 - 17:30 | Bioinformatics Training Room, Craik-Marshall Building | map | Ignacio Medina Castello, David Montaner, Marta Bleda |
2 | Tue 30 Sep 2014 09:30 - 17:30 | 09:30 - 17:30 | Bioinformatics Training Room, Craik-Marshall Building | map | Ignacio Medina Castello, David Montaner, Marta Bleda |
3 | Wed 1 Oct 2014 09:30 - 17:30 | 09:30 - 17:30 | Bioinformatics Training Room, Craik-Marshall Building | map | Ignacio Medina Castello, David Montaner, Marta Bleda |
The aim of this course is to familiarize the students with the latest analysis methodologies and to provide hands-on training on the analytical approaches implemented for RNA-seq data and whole exome variant analysis.
Presentations and practicals
A slightly longer version of this course is regularly offered as a part of "The Gulbenkian Training Programme in Bioinformatics". For further details of how to apply, see:
http://gtpb.igc.gulbenkian.pt/bicourses/
3
A number of times per year
Booking / availability