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CZE * ENG
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The CZECANCA Consortium has been created for the association of diagnostic and
research laboratories that are using the CZECANCA panel for the diagnosis of high-risk cancer patients.
Today, it represents a national platform of genetic laboratories sharing phenotype and genotype data and
creating a common database.
The consortium aims:
- Data sharing for the development of anonymized database of genotypes and phenotypes in
high-risk individuals and non-cancer controls analyzed by the CZECANCA panel,
- Functional characterization of selected VUS variants,
- Organization of regular workshops aiming at a unified interpretation of genotypes in Czech patients,
- Co-ordination of activities in international consortia (ENIGMA, CIMBA, BCAC, OCAC, ECAC).
| Participating laboratories: |
Contacts (activities): |
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001 | First Faculty of Medicine, Charles University and General University Hospital in Prague |
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002 | Masaryk Memorial Cancer Institute (MMCI) in Brno |
- Eva Macháčková (aboratory and data analysis, variant consensus)
- Lenka Foretová (genetic counseling, criteria adjustment)
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003 | AGEL laboratories |
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004 | GENNET |
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008 | GHC Genetics, s.r.o. |
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009 | Faculty Hospital in Pilsen |
- Monika Černá (laboratory and data analysis)
- Ivan Šubrt (clinical genetics)
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011 | Pronatal |
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012 | Faculty Hospital in Olomouc |
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013 | Hospital České Budějovice |
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014 | PRENET |
- Miroslav Fišer (laboratory and data analysis)
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015 | Ústav klinické a molekulární patologie a lékařské genetiky, FN Ostrava |
- Mgr. Lucie Faldynová (data analysis)
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016 | Genetika Plzeň |
- Mgr. Michaela Nečesánková,PhD (data analysis)
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| Other collaborators: |
Contact (activities): |
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| Laboratory of Cancer Cell Biology, IMG Czech Academy of Sciences |
- Libor Macůrek (functional analyses in vitro)
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| Department of Pediatrics and Inherited Metabolic Disorders (KPDPM) |
- Viktor Stránecký (bioinformatics, databases)
- Petr Nehasil (bioinformatics, databases, web)
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CZECANCA users’ workshops:
The workshops serve for regular exchange of users’ experiences with panel analysis, bioinformatics, and clinical
interpretation of genetic variants. The workshops become an important platform for laboratory workers,
bioinformaticians, clinical geneticists, and oncologists to unify/update national guidelines for germline genetic
testing of cancer predisposition and to unify/discuss further development of care of mutation carriers in Czechia.
Many activities exceeding the scope of germline genetic testing are realized in cooperation with other healthcare
professionals as well as with national healthcare professional societies including the Czech Society for Medical
Genetics and Genomics and Czech Society for Oncology
12. workshop (12. workshop (2024-05-16; Praha, 1. LF UK)
11. workshop (11. workshop (2023-02-14; Praha, 1. LF UK)
10. workshop (2022-05-17; České Budějovice, National conference of DNA diagnostics)
9. e-workshop (2021-11-30; on-line)
8. workshop (2021-06-09; Praha, 1. LF UK)
7. e-workshop (2020-11-10; on-line)
6. workshop (2019-12-12; Praha, IMG CAS)
5. workshop (2019-05-23; Plzeň, FN Plzeň)
4. workshop (2018-10-18; Ostrava, AGEL)
3. workshop (2018-02-13; Praha, 1. LF UK)
2. workshop (2017-05-15; Praha, GENNET)
1. workshop (2016-09-19; Brno, MMCI)
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