variation

This quick tip explores the new version of SNPeffect. For more information and links see http://blog.openhelix.eu/?p=10257

For more information about this resource see our blog post at URL http://blog.openhelix.eu/?p=10091. In today's tip I am going redo a movie originally done by Ensembl on SNP information in Ensembl, but I will use the updated Ensembl release 64.

For more information about this resource, please see our blog post at URL http://blog.openhelix.eu/?p=9933. In this tip I introduce users to the VnD, or genetic Variation and Drug database from the Korean Bioinformation Center, or KOBIC.

This week's tip is on using Galaxy to get flanking sequence. See http://blog.openhelix.eu/?p=9808 for more information.

A quick introduction to a web-based tool that allows you to correlate SNPs in a region with gene expression levels. See http://blog.openhelix.eu/?p=9275 for more details.

This tip is a quick introduction to PolySearch, for more information, see: http://blog.openhelix.eu/?p=9084

Today's tip is a quick introduction to the Gene Prioritization Portal. To find more information, see: http://blog.openhelix.eu/?p=8988

MutaDATABASE is a project to curate and organize human genomic variation of clinical significance. For references and links visit our blog post http://blog.openhelix.eu/?p=8688

Explore the new interface for the venerable OMIM genetics resource; visit http://blog.openhelix.eu/?p=8539 for more details and references.

A tip of the week on using SNPTips to view your 23andme data. For more information about the tool see http://blog.openhelix.eu/?p=7162