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
More information can be found here: http://blog.openhelix.eu/?p=4602 . This week's tip in 2nd part in a 5 part series of tips following one variation in an individual's genome across several databases and resources to find out what information we gather about the clinical association of that variation. This wee we look at dbSNP, VarView and OMIM.
For more information about this resource, see our blog post at http://blog.openhelix.eu/?p=4520. The Cancer Genome Workbench gathers cancer information from a wide variety of projects and presents the cumulative data as high-level summary visualizations. With just a bit of acclimation, researchers can utilize this resource to further their understanding of cancer genomics.
Mouse Resource Browser video tip: http://blog.openhelix.eu/?p=4501 In this week's tip, we present the MRB resource features and provide an overview of the structure. For more details about the resource and the paper that was published by the resource providers, click the URL for the OpenHelix blog entry for this tip.
You can read more at http://blog.openhelix.eu/?p=4455 . The first in a multi-part tour of the many resources available to the researcher or clinician looking into the data on genomic variation. Today's tip looks at UCSC Genome Browser and dbSNP.
A quick introduction to WAVe (Web Analysis of the Variome), a great tool that pulls in a wealth of information about human gene variation. For a more high-resolution version of this tip and more information about the resource, visit the OpenHelix blog.