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<biogps><data><item key="rating_data"><item key="avg_stars">0</item><item key="total">0</item><item key="avg">0</item></item><item key="name">Snap - a SNP Annotation Platform</item><item key="created">2011-08-29 23:03:39</item><item key="url">http://snap.humgen.au.dk/views/geneview.cgi?gene={{EnsemblGene}}</item><item key="lastmodified">2011-08-29 23:06:56</item><item key="usage_data"><item key="layouts">7.0</item><item key="users">5</item></item><item key="popularity">7.0</item><item key="owner"><item key="username">cwu</item><item key="url">/profile/2/cwu</item><item key="name">Chunlei Wu</item></item><item key="species"><item>human</item></item><item key="shortUrl">snap.humgen.au.dk</item><item key="id">951</item><item key="short_description">an integrated SNP annotation platform</item><item key="role_permission"><item>biogpsusers</item></item><item key="permission_style">public</item><item key="type">iframe</item><item key="options">None</item><item key="tags"><item>annotation</item><item>snp</item></item><item key="description">Snap is a sequence analysis tool providing a simple but detailed analysis of human genes and their variations. For each gene, a gene-gene relationship network can be generated based on protein-protein interaction data, metabolic pathway connections and extended through phylogenetic relations.
 
Snap provides tools for designing sequence primers and evaluating RNA splicing effects of single SNPs - known from the databases or defined by you. Primers can be designed for the amplification or sequencing of cDNA, genomic DNA, introns only or exons only.</item></data></biogps>
