Difference between revisions of "User:Armand"
| (3 intermediate revisions by the same user not shown) | |||
| Line 21: | Line 21: | ||
Bâtiment Génopode, UNIL | Bâtiment Génopode, UNIL | ||
1015 Lausanne, Switzerland | 1015 Lausanne, Switzerland | ||
| − | |||
| − | |||
e-mail: Armand.Valsesia AT licr.org | e-mail: Armand.Valsesia AT licr.org | ||
| Line 32: | Line 30: | ||
* A nice listing of software for Ultra High Throughput Sequencing Data ([[UHTS]]) | * A nice listing of software for Ultra High Throughput Sequencing Data ([[UHTS]]) | ||
| + | |||
| + | * some usefull unix commands ([[UNIX_recipes]]) | ||
| + | |||
| + | * how to package your matlab code ([[Packaging_matlab_to_standalone]]) | ||
| + | |||
| + | * how to deploy a VNC server ([[Vnc]]) | ||
Latest revision as of 17:47, 17 September 2009
Hi,
My name is Armand and I am a joint PhD student with Pr. Bergmann and Pr. Jongeneel.
My main interests are in detecting Copy Number Variation from micro-arrays (SNP arrays and CGH) and how such variation relates with the phenotype.
Some other projects I am also involved, include :
- studying the evolution and polymorphisms of some cancer-related genes.
- how to store structural variants in databases and how to visualize them.
Contact
Armand Valsesia
Ludwig Institute for Cancer Research
Bâtiment Génopode, UNIL
1015 Lausanne, Switzerland
e-mail: Armand.Valsesia AT licr.org
Some usefull links
- Running jobs on Vital-IT
- A nice listing of software for Ultra High Throughput Sequencing Data (UHTS)
- some usefull unix commands (UNIX_recipes)
- how to package your matlab code (Packaging_matlab_to_standalone)
- how to deploy a VNC server (Vnc)
