Register for the April 6th webinar: Using NCBI Databases with Tools that Predict Genomic Variant Effects

In two weeks, NCBI will give a demonstration of some open-source tools that use NCBI databases to predict effects of variants. We will begin with an overview of where to find and download data, particularly VCF and FASTA files, from NCBI, then show you how to use this data in 10 external tools that predict variant functional consequences, including ANNOVAR, PANTHER, SNAP-2, and CBIO MutationMapper.
Source: NCBI Announcements - Category: Databases & Libraries Source Type: news