Last week I
have competed the Synbreed Summer School called “Next Generation SequenceAnalysis: Practice and Departure to New Frontiers”. It was organized in Herrsching am Ammersee, Germany which is a place
just near Munchen. The main organizers were animal breeding people from
Technical University Munchen and researchers from the Helmholz Zentrum.
There were
several thing in the course that were “out of the ordinary”, yet contributed
for the course success (at least for my viewpoint).
1. Focus on practical data handling: I
liked this part very much. We went through everything, starting for the
installation of the software up to imputation. It is not easy, but manageable.
2. Usage of free software: I mean all software, including the operating
system. Actually I had to install the Ubuntu Linux because of this. But now I
am glad I did. The main interface is far from the command line feeling, which
often keeps people from installing Linux. At least with this new Ubuntu
graphical interface I had the feeling I am browsing a smartphone… Of course the
things can become pretty complicated, depending on the actual aims of the user,
but the basic navigation is without problems.
3. Course given by PhD students: I was
realizing this just by the end of the summer school. Not that PhD students are
not good enough (in fact they were excellent), but I would expect somebody
older “by default”. But I guess this was the strategy of the course to bring in
people who are working with these things on daily basis,as they are the most
qualified ones to introduce the techniques to us.
4. Evening sessions: After the daily workload
we often went for a beer-or-two, often ending in the billiard room. Good time!
Except from
the practical sessions there were also presenteres, who contributed
to afternoon sessions. They were specialist in their fields highlighting various possibilities of sequence data. The list is as follows: Mario Caccamo and Jared Simpson on De novo assembly, Paul Kersey on Genome browsers and databases, Ben Hayes
on Genomic selection, Agricultural genome
projects and Perspectives of using
sequence data, and last but not least Karl Schmid on Next generation population
genomics.
The list of
software and other useful links:
- Burrows Wheeler Aligner - for alligning short sequence reads
- SAMtools - various utilities to manipulate allignments
- SEQanswers - all-around forum for sequencing issues. They have a wiki too with the list of most popular software. If you are into sequencing, this is the place to dive deeper.
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