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. <br><br>
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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.<br>
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Some other projects I am also involved, include :<br>
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My main interests are in detecting Copy Number Variation from micro-arrays (SNP arrays and CGH) and how such variation relates with the phenotype.
<ul>
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<ol>- studying the evolution and polymorphisms of some cancer-related genes.</ol>
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Some other projects I am also involved, include :
<ol>- how to store structural variants in databases and how to visualize them. </ol>
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</ul>
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* 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:
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== 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
    Phone: + 41 21 692 40 66
 
    Fax:  + 41 21 692 40 65
 
 
     e-mail: Armand.Valsesia AT licr.org
 
     e-mail: Armand.Valsesia AT licr.org
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 +
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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]])
 +
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* how to package your matlab code ([[Packaging_matlab_to_standalone]])
 +
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* 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

  • A nice listing of software for Ultra High Throughput Sequencing Data (UHTS)
  • how to deploy a VNC server (Vnc)