Difference between revisions of "User:Armand"
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== Some usefull links == | == Some usefull links == | ||
| − | * Running jobs on | + | * 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
- Running jobs on Vital-IT
- A nice listing of software for Ultra High Throughput Sequencing Data (UHTS)
