NCBI Minute: Variant Interpretation Using NCBI Resources

Presented November 14, 2018.
This webinar shows you how to use NCBI’s genome browsers for variant interpretation. The graphical displays of thee Genome Data Viewer (GDV) and Variation Viewer offer an interactive experience that allows you to explore NCBI’s rich collection of annotations, datasets and literature for deciphering your variant-associated data. We step through case studies and show you how to quickly display relevant NCBI track sets - including the new RefSeq Functional Elements track, upload a file or remotely-hosted dataset and display these data as a track, and use browser tracks to identify known variants, then assess variant significance (functional and clinical) and allele frequency. You will also learn how to navigate from the browser to NCBI resources such as ClinVar, dbSNP and PubMed, for additional variant information.
Websites used in this webinar:
www.ncbi.nlm.n...
www.ncbi.nlm.n...
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[@BeccAcCardenas]

Love this break down. Thanks!! Now if only the filter wouldn't lead to me researching even MORE genes. Science LOVE.🤘🏻

[@karthikeyang2037]

how can i download all the variants with their key variations like Met1Arg in a single file???

[@kabirmustafa10]

User:ZScout370