Objective
Cytogenetics has made major contribution to the understanding of chromosomal basis of constitutional and acquired diseases. They are widely applied in clinical practice for the diagnosis, prevention and treatment of severe conditions such as cancer and genetic diseases. They are also used for monitoring biological effects of mutagenic and carcinogenic agents such as chemicals and radiation.
In recent years a new technique has developed in Western Europe that extends the capabilities of cytogenetics to the molecular level: the field of molecular cytogenetics. Using labelled nucleic acid probes it is possible to specifically mark multiple DNA targets in meta- and interphase nuclei, such that the marked regions can be visualized with the aid of fluorescence or brightfield microscopy. Deviations from the normal pattern of hybridization permit the identification of genetically aberrant cells. This new ability has major impact in areas such as prenatal diagnosis, oncology, hematology, pathology and genetic toxicology.
The number of cells that must be examined to reach a reliable decision on the molecular cytogenetic make-up of a cell sample, the complexity of the images and the amount of analysis time available, clearly indicate that instrumentation for the (semi) automated examination of microscope images is crucial to achieve the required objectivity and speed. This has been the driving force for proposing the Concerted Action "Automation of Molecular Cytogenetic Analyses" (CA-AMCA).
Given the universal applicability of these biomedically important methodologies, there is a similar need in the NIS countries, but in these countries there exists an information gap regarding implementation and further development of the in situ hybridization methodology and its associated microscopies as well as regarding the image acquisition, -processing and -analyses techniques.
The objective of this proposal is, therefore, to enable the participating groups to efficiently help filling their currently existing information gap and to contribute to reaching the original goals of the CA-AMCA with specific scientific input from their national perspectives by using the channels provided by the existing CA-AMCA.
Fields of science (EuroSciVoc)
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Programme(s)
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Topic(s)
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Call for proposal
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Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
Funding Scheme
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Coordinator
2333 AA Leiden
Netherlands
The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.