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V předvečer Světového dne vzácných onemocnění dne 27. února 2023 uspořádalo České centrum pro fenogenomiku při Ústavu molekulární genetiky AV ČR s partnery diskusi předních odborníků k tématům vzácných onemocnění v prostorách Magenta Experience Centre na Praze 4. Cílem akce bylo představit široké veřejnosti problematiku vzácných onemocnění z pohledu vědců v základním výzkumu, lékařů a pacientských organizací a vznik… Read more

Applications for innovative proposals to harness canSERV´s unified oncology services launches this week. A first of its kind, the largest European-wide consortium of research infrastructures is offering free-of-charge transnational access to cutting-edge services to develop breakthrough personalised cancer treatments. The complexity of cancer requires a multidisciplinary treatment approach, integrating patient- and tumour-specific information at different… Read more

Human Diseases Models Morphological Phenotyping (MorphoPHEN) consists of an integrated and interdisciplinary Erasmus Mundus Joint Master. It is conceived to alleviate the real shortage of experts in morphological mouse phenotyping, which is needed to generate a positive impact of preclinical biomedicine and improve human translatability (from the bench to the bedside). MorphoPHENis a one-year Erasmus… Read more

More than ten million sequences of the SARS-CoV-2 coronavirus had to be examined by an international team of scientists to find universal weaknesses of coronaviruses that do not change even with frequent mutations and the emergence of new variants. Analysis of patient samples then revealed rare antibodies that block all previously known SARS-CoV-2 variants, as… Read more

Are you interested in our preclinical services? Download our latest leaflet with an overview of services we provide to our users in the area of preclinical services. Read more

The Czech Academy of Sciences celebrates 70 years. Genetically modified mouse models help reveal the causes of human diseases, explains scientist Radislav Sedláček. Just turn off a gene in a mouse and you will learn which gene could be responsible for one of the diseases in humans. In the next part of our series on… Read more

“Gene Age” is an accompanying travelling lecture series of the AV21 Strategy research programme “Towards precision medicine and gene therapy “ In December 2022, the Czech Centre for Phenogenomics (CCP) at the Institute of Molecular Genetics of the Czech Academy of Sciences organized a traveling series of lectures “The Gene Age” on the topic of… Read more

We would like to inform you about a new range of transnational access calls recently launched under the ISIDORe project. These are free-of-charge open calls on specific pathogens and related-services accessible to researchers in the EU and abroad. Details about the open calls are available at ISIDORe website. Find out more about how INFRAFRONTIER contributes… Read more

Global and European Infrastructures IMPC and INFRAFRONTIER Towards the Deciphering of Gene Functions for Human Health 18 October 2022, 13:00 – 15:00  Hybrid event (Brno, Czech Republic + Zoom) European and world-wide research infrastructures such as IMPC and INFRAFRONTIER will provide comprehensive resources to unravel gene function in physiology and disease. These infrastructures are used… Read more

The Nobel Prize in Physiology or Medicine 2022 was awarded to Svante Pääbo “for his discoveries concerning the genomes of extinct hominins and human evolution”. More information here. Svante Pääbo from Max Planck Institute for Evolutionary Anthropology in Leipzig, Germany, uses research services of the Czech Centre for Phenogenomics, and was a keynote speaker at… Read more