Smp: Dna
نویسندگان
چکیده
Introduction The diversity of the human genome is a decisive factor in the causation and pathogenesis of complex disease as well as for the individual response to biologically active substances (pharmacogenomics). A key step in all strategies for disease gene identification is the comparative sequence analysis of candidate genes in patients and controls to identify those specific sequence variations associated with complex disease. The two laboratories involved in this subproject (MPIMG, Berlin and FLI, Jena) have installed a roboter based automated high-throughput resequencing service platform open to all members, cooperating in NGFN (Fig.1, Fig. 2).
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