Difference between revisions of "User:Armand"

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== Some usefull links ==
 
== Some usefull links ==
  
* Running jobs on Vital-IT [http://www2.unil.ch/cbg/index.php?title=Vital-IT]
+
* Running jobs on [[Vital-IT]]
  
 
* A nice listing of software for Ultra High Throughput Sequencing Data ([[UHTS]])
 
* A nice listing of software for Ultra High Throughput Sequencing Data ([[UHTS]])

Revision as of 17:08, 7 April 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
    Phone: + 41 21 692 40 66
    Fax:   + 41 21 692 40 65
    e-mail: Armand.Valsesia AT licr.org

Some usefull links

  • A nice listing of software for Ultra High Throughput Sequencing Data (UHTS)