7TH MYELOMA WORKSHOP MODERN TECHNOLOGIES IN

7TH MYELOMA WORKSHOP:
DETECTION OF CELL CLONES
IN MULTIPLE MYELOMA
PROGRAM:
OCTOBER 17, 2012
THEORETICAL PART
9:00 - 9:40
Registration &
Breakfast
09:45
Roman Hájek:
Introduction
10:00
Bruno Paiva:
High-throughput immunophenotypic expression profiling
of myeloma cells: insight into disease pathogenesis
and chemoresistance
10:30
Christian Langer:
The role of microRNA for the development of plasma cell
disorders in the context of other genetic changes
11:00
Sabina Ševčíková:
11:20
Lucie Říhová:
MicroRNA in multiple myeloma
Plasma cell phenotype in multiple myeloma – retrospective
data analysis
11:45 - 13:10
Lunch
13:15
Lorenzo Melchor:
13:45
Elena Dementyeva:
Unravelling the intraclonal hetorogeneity of multiple
myeloma using next generation sequencing and single cell
analysis
Clinical implication of CA and expression of centrosomal
functional genes in multiple myeloma
Coffee Break
14:15 - 14:55
15:00
Martin Schmidt-Hieber:
15:30
Andreas Beilhack:
16:00 – 17:00
19:30
Cytogenetic heterogeneity in plasma cell dyscrasias
Multiple myeloma mouse models to visualize disease
progression and response to therapy
Discussion
Social event
PROGRAM:
7TH MYELOMA WORKSHOP:
OCTOBER 18, 2012
9:00 - 17:00
DETECTION OF CELL CLONES
IN MULTIPLE MYELOMA
PRACTICAL PART
A: FLOW CYTOMETRY
9:30 – 11:30
Lucie Říhová:
Standardization of flow cytometry within Czech Myeloma Group
12:30 – 16:30
Lucie Říhová:
Implementation of Euroflow PCD Panel - Standard Operation
protocol and MRD Manual
B: GENOMIC PROFILING USING CGH +
SNP MICROARRAY PLATFORM IN
MEDICAL GENETICS AND ONCOLOGY
LECTURES
9:00 – 11:00
Introducing combined CGH and SNP arrays for cancer
characterisation and a unique next-generation sequencing service.
Ruth Burton:
Oxford Gene Technology
Array CGH in preimplantation genetic diagnosis/preimplantation
genetic screening: our experience and first results
Kristina Beránková et al.:
Brno
FISH vs. Array-CGH in multiple myeloma: a single Czech center
experience
Jan Smetana et al.:
Brno
Roundtable discussion - meet the expert:
A. Beilhack, L. Melchor, M. Schmidt-Hieber
Coffee Break
9:45 - 10:10
Pavla Mičková et al.:
Olomouc
Vladimíra Vallová et al.:
Brno
Studium chromosomových a genových změn u souboru nemocnych s
MM s t(14;16) s využitím čipových technologií
Využití array CGH pro určování genetických změn u karcinomu
děložního hrdla
Diana Grochová et al.: Array CGH v prenatální diagnostice: detekce velkých přestaveb v
Brno genomu, které konvenční cytogenetika neodhalila
Lunch
11:30 - 12:30
PRACTICAL PART
12:30 – 17:00
Jan Smetana &
Romana Zaoralová:
Brno
WHOLE GENOME SCANNING BY CGH AND SNP ARRAYS IN
ROUTINE CYTOGENETIC DIAGNOSTICS - INTERPRETATION OF
STRUCTURAL GENOME VARIANTS