Tip of the Week: Canonical gene information

submitted by: OpenHelix

Today's tip of the week is how to get canonical gene information using the UCSC Genome and Table Browsers. For more information see the blog post

Tip of the Week: VISTA Enhancer Browser Database

submitted by: OpenHelix

Computational comparative genomics data translated to a terrific lab-based in vivo follow-up. Visit http://blog.openhelix.eu/?p=5814 for details and references.

Tip of the Week: iTol

submitted by: OpenHelix

Our latest weekly tip on the Interactive Tree of Life, iTOL. You can find out more at our blog

Tip of the Week: BioExtract

submitted by: OpenHelix

This week's tip is on BioExtract. See the blog post more information about BioExtract and other similar tools

Tip of the week: CTD and VennViewer

submitted by: OpenHelix

For more description and information go to: http://blog.openhelix.eu/?p=5488 This tip of the week is on Comparative Toxicogenomics Database or CTD and the new tool VennViewer.

Tip of the Week: PathCase for pathway data

submitted by: OpenHelix

Explores PathCase visualization of pathway data. For details http://blog.openhelix.eu/?p=5414 visit our blog, where links and a reference for the resources is also provided.

Tip of the Week: Galaxy Pages

submitted by: OpenHelix

Find more here about this tip: http://wp.me/pDP1I-1mI This tip of the week introduces you to Galaxy Pages, an annotation and description creator for genomics analysis

RGenetics at Galaxy

submitted by: OpenHelix

Visit our blog for more info on this tip: http://blog.openhelix.eu/?p=4899 A tip introducing Rgenetics at Galaxy

Tip of the Week: MINT, Molecular INTeractions Database

submitted by: OpenHelix

Learn more about MINT from our blog http://blog.openhelix.eu/?p=4778 . In this tip of the week we explore the basic search and visualization features of the MINT resource for protein-protein interactions.

Tip of the Week: Genome Variation Tour III

submitted by: OpenHelix

For more information, few the blog post at: http://blog.openhelix.eu/?p=4763 . This tip is the continuation of a genome variation tour. We will look at finding SNPs in LD with our SNP of interest using GVS