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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):
001 First Faculty of Medicine, Charles University and General University Hospital in Prague
002 Masaryk Memorial Cancer Institute (MMCI) in Brno
  • Eva Macháčková (aboratory and data analysis, variant consensus)
  • Lenka Foretová (genetic counseling, criteria adjustment)
003 AGEL laboratories
004 GENNET
008 GHC Genetics, s.r.o.
009 Faculty Hospital in Pilsen
  • Monika Černá (laboratory and data analysis)
  • Ivan Šubrt (clinical genetics)
011 Pronatal
012 Faculty Hospital in Olomouc
013 Hospital České Budějovice
014 PRENET
  • Miroslav Fišer (laboratory and data analysis)
015 Ústav klinické a molekulární patologie a lékařské genetiky, FN Ostrava
  • Mgr. Lucie Faldynová (data analysis)
016 Genetika Plzeň
  • Mgr. Michaela Nečesánková,PhD (data analysis)
Other collaborators: Contact (activities):
Laboratory of Cancer Cell Biology, IMG Czech Academy of Sciences
  • Libor Macůrek (functional analyses in vitro)
Department of Pediatrics and Inherited Metabolic Disorders (KPDPM)
  • Viktor Stránecký (bioinformatics, databases)
  • Petr Nehasil (bioinformatics, databases, web)


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)