in the article "DNA copy number aberrations in breast cancer studied by array Comparative Genomic Hybridization" in the journal of Genomics, Proteomics & Bioinformatics. The deposited data for the paper "An improved method for genome wide DNA methylation profiling correlated to transcription and genomic instability in two breast cancer cell lines" published in BMC Genomics |
INTRODUCTION
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.
Reference: Li, S., Ma, L., Li, H., Vang, S., Hu, Y., Bolund, L., Wang, J. "Snap: an integrated SNP annotation platform." Nucleic Acids Res. 2007 Jan 1; vol: 35 (Database issue): D707-10 (NAR pdf tables)
Snap v3.4 released - 2008-07-07 Snap v3.2 released - 2007-01-29
E-mail: snap@humgen.au.dk; snap@genomics.org.cn
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Last Update: 2008-07-07 18:00 Email: snap@humgen.au.dk; snap@genomics.org.cn