[BBC] N2N seminar Thursday, January 29 at 11 am: 'Bioinformatics in cancer research' By Prof. van Loo

[Katrijn Vannerum]

Dear All,

Prof. Peter van Loo will give a seminar on Thursday, January 29 at 11 am: 'Bioinformatics in cancer research'. (See abstract below)

Please contact me if you would like to have a meeting with Prof. Peter van Loo in the afternoon.
The lunch meeting is open to all PhD students, but lunch is only provided for students registered at the Doctoral Schools. Registration is still possible.

With kind regards,

Katrijn Vannerum

PhD
Project manager
N2N (From Nucleotides to Networks)
Multidisciplinary Research Partnership
Bioinformatics and Systems Biology
Ghent University
http://www.nucleotides2networks.be/
twitter: @N2N_UGent
Katrijn.Vannerum at UGent.be<mailto:Katrijn.Vannerum at UGent.be>
Technologiepark 927
9052 Gent, Belgium
+32 (0)9 331 36 85


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"Bioinformatics in cancer research"

Professor Peter van Loo
KU Leuven, Department of Human Genetics, Leuven, Belgium

January 29, 2014 (11:00)
Lunch meeting for Doctoral Schools students 12:00-14:00
Jozef Schell seminar room, Technologiepark 927 - 9052 Zwijnaarde
http://www.nucleotides2networks.be/node/232
http://www.nucleotides2networks.be/events
Abstract
Cancer evolves dynamically as clonal expansions supersede one another, driven by shifting selective pressures, mutational processes, and disrupted cancer genes. These processes mark the genome, such that a cancer's life history is encrypted in the somatic mutations present. We are developing algorithms to decipher this narrative from whole genome sequencing data and are applying them to several cancer types. We call such approaches "molecular archaeology of cancer", as we are using genomics and bioinformatics algorithms to infer a tumour's evolutionary history. I will discuss applications of our methods to breast cancer, allowing us to disentangle subclonal architecture from whole genome sequencing data, as well as time events such as chromosome duplications along a tumour's lifetime. In addition, I will describe how extending these molecular archaeology approaches to multiple sampling studies allow enhanced and unique insights into cancer evolution, and I will illustrate that using genomics studies on prostate cancer metastases, where we are able to elucidate the patterns of metastatic spread in unprecedented detail.

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