---------- Forwarded message ---------- From: Public announcements regarding dbSNP <[email protected]> Date: Tue, May 12, 2015 at 12:50 PM Subject: [dbsnp-announce] Reminder: dbVar Webinar Tomorrow (May 13, 2015)
Please register for Explore Copy Number and Other Structural Variants in dbVar, NCBI Database of Large-Scale Genetic Variation on May 13, 2015 1:00 PM EDT at: https://attendee.gotowebinar.com/register/3038276448844084738 dbVar is NCBI's database of genomic structural variation. dbVar includes inversions, balanced translocations and the genomic imbalances known as copy number variants (CNVs). dbVar serves as a permanent archive of reported structural variation and provides integration of that data with NCBI’s large variety of bioinformatics tools and variation resources. After a brief introduction to dbVar, this webinar will show you how to display clinically relevant CNVs stored in dbVar using the dbVar Genome Browser and to uploading your own CNV data to view alongside the dbVar variation. After registering, you will receive a confirmation email containing information about joining the webinar.
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