He Molecular Pathology Laboratory was established in 2000 in an attempt to study, diagnose and understand diseases at the molecular level specifically utilizing the uniqueness of the Arabian genome for this purpose. Visit our Private Laboratory and Genomic Medicine Clinic Today. New Discoveries from our laboratory. We have recently found yet another reason why cells become resistant to chemotherapy when RKIP is lost or diminished in ex.

Skip to EBI global navigation menu. Part of the European Molecular Biology Laboratory. The home for big data in biology. 3 Apr 2017 - 6 Apr 2017. 4 Apr 2017 - 4 Apr 2017.

Is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population. FinDis provides up-to-date information on the 36 monogenic diseases belonging to the Finnish disease heritage. Prevalence or incidence and a short description of clinical symptoms. Genetic locus and a molecular description for identified mutations. Disease allele frequencies typically reported for Finnish mutations. Read About the FinDis project.

Welcome to the G2P Knowledge Centre. Welcome to the G2P Knowledge Centre - home of the GEN2PHEN project, a holistic approach to genotype-to-phenotype data. Find out more about GEN2PHEN. See a list of GEN2PHEN-supported activities, resources, platforms and initiatives. A simple gene search for G2P data. A listing of locus-specific databases.

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Welcome to the Mutalyzer website. The aim of this program suite is to support checks of Sequence Variant Nomenclature. According to the guidelines of the Human Genome Variation Society. The Name Checker takes the complete sequence variant description as input and checks whether it is correct. Takes the complete sequence variant description as input and checks whether the syntax is correct.