Tip of the Week: Getting flanking sequence of genomic locations

submitted by: OpenHelix

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

Tip of the Week: MutaDATABASE

submitted by: OpenHelix

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

Tip of the Week: SNPTips and viewing your personal genomic data

submitted by: OpenHelix

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

Tip of the Week: SIFT: Sorting Intolerant (SNPs) From Tolerant

submitted by: OpenHelix

Today's Tip of the Week is a quick intro to SIFT, find more information at: http://blog.openhelix.eu/?p=7098

Tip of the Week: PolyPhen

submitted by: OpenHelix

This week's tip is on PolyPhen, a predictor of nonsynonymous SNP impacts on protein functions. For more information about PolyPhen and SNP functional prediction see the blog post: http://blog.openhelix.eu/?p=6867

Tip of the Week: WAVe

submitted by: OpenHelix

Web Analysis of the Variome. For more information see our blog post: http://blog.openhelix.eu/?p=4319

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.

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: 1000 Genomes Browser

submitted by: OpenHelix

This 1000 Genomes Project tip can be found http://blog.openhelix.eu/?p=4830 , with additional information about the project and some references associated with the project.

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