User:Armand

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.

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Contact

    Armand Valsesia
    Ludwig Institute for Cancer Research
    Bâtiment Génopode, UNIL
    1015 Lausanne, Switzerland
    Phone: + 41 21 692 40 66
    Fax:   + 41 21 692 40 65
    e-mail: Armand.Valsesia AT licr.org

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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)