CNVannotator-处理拷贝数变异的！

Jimmy

http://bioinfo.mc.vanderbilt.edu/CNVannotator/所有的下载资源在：http://bioinfo.mc.vanderbilt.edu/CNVannotator/database/
CNVannotatorIntegrative annotation of copy number variations in humans

• 1. Filter 356,817 common and 181,261 disease CNVs.
• 2. Overlap with 2,864,501 known variants from genome-wide association studies and gene fusion events with phenotypes.
• 3. Perform discovery on 2,013,344 genomic features, including ENCODE regultory element, segmental duplication, promoter, enhancer, methylation sites, and transcription factor binding sites.
• 4. Create cancer-specific annotations for 716 tumor suppressor genes and 263 oncogenes for CNVs.
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Please cite: Zhao M, Zhao Z (2013) CNVannotator: a Comprehensive Annotation Server for Copy Number Variation in the Human Genome. PLoS ONE 8(11):e80170Article online   PumMed

惠真-市二医院

这个好，mark下！