Difference between revisions of "User:Armand"
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Hi, | Hi, | ||
| − | My name is Armand and I am a joint PhD student with Pr. Bergmann and Pr. Jongeneel. | + | 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 : | + | 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. | ||
| + | |||
| Line 13: | Line 16: | ||
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| − | Contact | + | == Contact == |
Armand Valsesia | Armand Valsesia | ||
Ludwig Institute for Cancer Research | Ludwig Institute for Cancer Research | ||
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 | ||
---- | ---- | ||
| − | Some usefull links | + | == 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]]) | |
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)
