From | 2009-10-18 |
To | 2009-10-22 |
Course | Cytogenetics witnessed, in recent years, a series of technological innovation that forced the field to completely and repeatedly renew its approach and vision of chromosomal imbalances and copy number variation in the population, in cancer and in evolution. Molecular cytogenetics, microarray-CGH, and massive sequencing technologies are the most relevant techniques that trigged these changes. The Course is designed to give a broad overview of these technologies and to discuss with attendants the way they could integrate each other in a modern genetic/cytogenetic laboratory. |
Venue | EuroMediterranean University Center of Ronzano |
Directors | M. Rocchi (Bari, Italy), F. Mitelman (Lund, Sweden), B. Young (London, UK) |
Speakers | G. Calabrese (Chieti, Italy), M. Cremer (Munich, Germany), W. Chen (Berlin, Germany), S. Debernardi (London, UK), G. De Bellis (Segrate, Italy), N. Gilbert (Edinburgh, UK), F. Speleman (Ghent, Belgium), Andrew Sharp (Geneva, CH), R. Stanyon (Florence, Italy), R. Ullmann (Berlin, Germany), J. Vermeesch (Leuven, Belgium), B. Ylstra (Amsterdam, The Netherlands), O. Zuffardi (Pavia, Italy) |
Programme | Sunday, October 18
Morning Session
08:30
REGISTRATION
09:00
O. Zuffardi
Cytogenetics
10:00
M. Rocchi
Human genome plasticity
10:45
COFFEE BREAK
11:15
F. Mitelman
Cancer cytogenetics
12:45
Lunch break
Afternoon Session
14:30
R. Stanyon
Evolution and origins of the human karyotype
15:15
Workshop:
Resources for molecular cytogenetics (M. Rocchi)
16:15
Coffee break
16:30
Workshop:
FiberFISH (G. Calabrese)
Monday, October 19
Morning Session
09:00
B. Ylstra
Introduction to microarrays
09:30
A. Sharp
Copy Number Variation
10:30
COFFEE BREAK
11:00
O. Zuffardi
CNV in clinics
11:45
B. Ylstra
ArrayCGH: from technique to patient treatment
12:30
Lunch break
Afternoon Session
14:30
F. Speleman
QPCR platform for miRNA and TUCR gene profiling
15:15
Workshop:
QPCR-miRNA(F. Speleman)
16:15
Coffee break
16:30
Workshop:
Oligo microarray (B. Ylstra)
Tuesday, October 20
Morning Session
9:00
F. Speleman
Integrated genomics for disease gene discovery
09:45
B. Young
The application of SNP arrays to the cancer genome
10:30
COFFEE BREAK
11:00
B. Young
Expression profiling by Microarray
11:45
J. Vermeesch
Genome wide CNV and SNP detection in single cells
12:30
Lunch break
14:00
Free afternoon
Optional sightseeing/shopping tour in Bologna
Wednesday, October 21
Morning Session
09:00
G. De Bellis
Introduction to massive sequencing: the 454 approach
09:45
W. Chen
Application of Illumina/Solexa sequencing technology in genetic research
10:30
COFFEE BREAK
11:00
R. Ullmann
How next generation sequencing benefits from molecular cytogenetic technique
11:45
S. Debernardi
miRNA expression (by massive sequencing)
12:30
Lunch break
Afternoon Session
14:30
G. De Bellis
Mutation scanning by massive sequencing
15:15
Workshop:
Solexa sequencing technology (W. Chen)
16:15
Coffee break
16:30
Workshop:
454 sequencing technology (G. De Bellis)
Thursday, October 22
Morning Session
09:00
N. Gilbert
Epigenetics
09:45
M. Cremer
Nuclear architecture- an epigenetic mechanism for the regulation of nuclear functions
10:30
COFFEE BREAK
11:00
A. Sharp
Human imprinted genes
12:30
Lunch
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