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Webinar of the Month Find Significant SNPs in Your Samples SNP verification and prioritization is one of the most time consuming tasks in variant analysis. Avadis NGS 1.3 includes numerous changes to make end-to-end SNP analysis easy and intuitive. The SNP detection algorithm has been enhanced to improve accuracy. The reporting format has been changed to enable easier downstream filtering of variant alleles. Utility methods for importing and comparing variant allele lists are provided to allow researchers to quickly check which known SNPs of interest are present in the samples. The variant support view has been incorporated into the genome browser itself to enable easier verification. In addition to these enhancements, Webinar attendees will learn how to use the new "Find Significant SNPs" analysis workflow. This workflow supports multiple experimental setups and can be used for quickly identifying population-specific variants, somatic mutations, and tumor-specific markers via an intuitive graphical user interface.
We have scheduled one session for North and South America, and a different session for Europe and Asia. Choose the webinar time that suits you best and register for free! See you at the webinar! - The Avadis NGS Team |
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