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Czech Centre for Phenogenomics
Institute of Molecular Genetics of the Czech Academy of Sciences
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Model Generation
Genome Engineering & Model Generation
Genotyping and Breeding, Cryopreservation & EMMA/Infrafrontier Services
Animal Facility
Phenotyping
Biochemistry & Haematology
Bioimaging & Embryology
Cardiovascular
Vision
Hearing & Electrophysiology
Histopathology
Immunology
Lung Function
Metabolism
Neurobiology & Behaviour
Metabolomics
PDX & Cancer Models
Models of Infectious Diseases (BSL-3)
Biostatistics / Bioinformatics
Database of IMPC Lines Created at CCP
Interactive Presentations of Phenotyping Data
Preclinical Testing
Available Standardized Modalities & Key Services
Preclinical Tests Already Implemented
Partner Projects
Cooperation with Industry
Rare Disease Factory
Rare Diseases
Harlequin Ichthyosis
Achondroplasia
Hyperphosphatemic Familial Tumoral Calcinosis (HFTC)
Canavan Disease
RASopathies
Diamond-Blackfan Anemia
Liang-Wang Syndrome
SPATA5
PACS2-related EIDEE
Kleefstra-like Syndrome
Netherton Syndrome
Angelman Syndrome
Prader-Willi Syndrome
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