Informace o projektu
MEDGENET - Medical genomics and epigenomics network
(MEDGENET)
- Kód projektu
- 692298
- Období řešení
- 1/2016 - 12/2018
- Investor / Programový rámec / typ projektu
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Evropská unie
- Horizon 2020
- Spreading excellence and widening participation
- Fakulta / Pracoviště MU
- Středoevropský technologický institut
- Spolupracující organizace
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European Molecular Biology Laboratory
Uppsala universitet
Ethniko Kentro Erevnas Kai Technologikis
The main goal of MEDGENET consortium is to use synergies and existing expertise in EU leading institutions such as EMBL, Uppsala University and CERTH to reinforce the productivity and competitiveness of the CEITEC in the field of medical genomics and epigenomics. We propose clear strategy based on combination of unique complementary skills present in partner institutions that will transform CEITEC into a key leader in the field. ERA Chair who recently joint CEITEC already initiated the transformational change of the institute and TWINNING framework will further support sharing her international contacts with other CEITEC researchers. MEDGENET aims to create well-educated taskforce of biomedical researchers, who will notably contribute to the development of new genomics and bioinformatics tools and their application in clinical practice. Proposed project will enable to establish the best practices for performing innovative and high-quality biomedical research and to strengthen CEITEC´s competence to translate the research results into high value-added clinical applications. Stimulation of knowledge exchange, implementation of cutting edge technologies and mastery of modern genomics and bioinformatics methodologies will have a direct impact on the overall research and innovation potential of CEITEC and will increase its visibility in the international scientific community.
Publikace
Počet publikací: 53
2016
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ATM mutations in major stereotyped subsets of chronic lymphocytic leukemia: Enrichment in subset 2 is associated with markedly short telomeres
Haematologica, rok: 2016, ročník: 101, vydání: 9, DOI
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B cell receptor signaling activity is associated with evolution of TP53 defects in chronic lymphocytic leukemia
Rok: 2016, druh: Konferenční abstrakty
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Cancer clonal evolution and mutational patterns in leukemia patients and development of software for variant calling.
Rok: 2016, druh: Konferenční abstrakty
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Decreased expression of WNT3, a canonical Wnt pathway ligand is frequent in chronic lymphocytic leukemia progression and identifies patients with short treatment-free survival in mutated IGHV
Rok: 2016, druh: Konferenční abstrakty
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Detailed analysis of chronic lymphocytic leukemia cases with single TP53 mutation
Rok: 2016, druh: Konferenční abstrakty
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Ibrutinib inhibits CD20 up-regulation on CLL B cells mediated by the CXCR4/SDF-1 AXIS.
Rok: 2016, druh: Konferenční abstrakty
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Introduction of nanopore sequencing to genomic core facility RNA workflows
Rok: 2016, druh: Konferenční abstrakty
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Low-Burden TP53 mutations occur in chronic phase of myeloproliferative neoplasms regardless of hydroxyurea administration, disease type and JAK2 status
Rok: 2016, druh: Konferenční abstrakty
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MicroRNAs in the microenvironmental interactions of B cell leukemias.
Rok: 2016, druh: Konferenční abstrakty
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Monoallelic TP53 abnormalities in CLL: do they really exist? The frequency and clinical impact of copy-neutral loss of heterozygosity
Rok: 2016, druh: Konferenční abstrakty