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Databases, Resources and Tools

Aims

The overall objective of Work package 2 is to provide the genetic healthcare workers, the end-users and the health care authorities with a portfolio of quality-assured information sources and informatics tools that are subject to validation and quality procedures.

The second major objective is to avoid duplication and ensure consistency and inter-operability of databases in the field of genetic testing.

The databases which will be considered are databases on genetic diseases, genetic tests, mutation databases and sequence databases.

The third major objective is to improve the quality of existing information services. Many groups have produced guidelines for quality standards in health information on the web. It is time to transpose these guidelines in the Human Genetics Database field and to promote their respect by the database producers.

General Information


State of the art 2005 (EuroGentest1-Unit 2)
State of the art of information databases and knowledge bases across Europe can be found here

Orphanet Formal partnership with EuroGentest Exit this website

OrphanetExit this website is a database of rare diseases, which was designed to assist in diagnosing and treating rare diseases, as well as to further clinical research. It has been selected to serve as the central database of the EuroGenTest network. You can find information on:

  • diseases, tests, laboratories, professionals, support groups, organisations
  • and much more...

News

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Events

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Mar 2005 - Unit 1 - Database labs

Paris (FR) More...

Feb 2006 - Database Expert Group (WP1.2 + WP2.1)

Paris (FR) More...

Feb 2006 - Expert meeting on collecting and maintaining QAu data for biochemical labs (WP2.1 and WP1.5)

Paris (FR) More...

Last changed: 2011-04-01


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