Nikos Krypides of the DOE Joint Genome Institute discusses metagenomics and the challenge of dealing with terabases of data on June 4, 2010 at the "Sequencing, Finishing, Analysis in the Future" meeting in Santa Fe, NM.
Bob Fulton of Washington University discusses the sequencing platforms in use at this large scale genome center on June 2, 2010 at the "Sequencing, Finishing, Analysis in the Future" meeting in Santa Fe, NM.
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.
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.