News

11–12 September 2025 · Prague, Czech Republic
The conference focuses on rare diseases and gene therapy research, bringing together a diverse community of experts to advance the field. Read more

We are seeking a motivated postdoctoral scientist or junior researcher focused on Prader-Willi syndrome research and therapy development. Read more

To strengthen our team working on preclinical R & D projects related to skin diseases, we are seeking an experienced researcher or postdoctoral scientist. Read more

The Czech Centre for Phenogenomics (CCP) offers an exciting opportunity for an experienced and motivated expert to lead the Transgenic and Archiving Module. Read more

We cordially invite you to the traditional science fair. INTERACTIVE EXHIBITION FOR CHILDREN AND ADULTS CHILDREN’S ZONE Little scientists and curious people will try pipetting, gluing cells, logic games, observing sperm under a microscope and a fun photo corner in a protective suit from a BSL3 laboratory. PHENOTYPING TEST STATION Explore the process of scientific… Read more

We’re running a VisualSonics workshop for the new F2 on28 May. In the morning we’ll have a few short talks in the seminar room, and after lunch you can get hands-on and try out the system yourself. Application specialist will also be around on 29 May at the CCP to show any specific measurements you’re… Read more

České centrum pro fenogenomiku (CCP) hledá motivovaného a zodpovědného kandidáta na pozici Projektového manažera. Read more

The program of conference TT2025 (https://tt2025.org/programme/) also included the presentation of the lecture award Orbis Pictus given by the Czech Centre for Phenogenomic. This year was awarded the lecture of Professor Anna-Katerina Hadjantonakis, Chair of Developmental Biology Program, Sloan Kettering Institute, New York, USA. Read more

CCP is happy to provide large porfolio of phenotyping and preclinical services to research community. Read more

Hope for patients affected by SPATA5 disease in CCP: https://archiv.hn.cz/c1-67711270-v-cesku-odstartoval-unikatni-vyzkum-vzacne-geneticke-poruchy-iniciovali-ho-rodice-deti-s-touto-diagnozou Read more