De Novo Genome Sequencing of the Venturia inaequalis (apple scab) Using the Illumina Genome Analyser

submitted by: dougramsey

De Novo Genome Sequencing of the Venturia inaequalis (apple scab) Using the Illumina Genome Analyser presented by Jasper Rees, University of the Western Cape, South Africa

De Novo Assembly of Short Reads as a Discovery Tool

submitted by: dougramsey

De Novo Assembly of Short Reads as a Discovery Tool presented by Inanc Birol, BC Cancer Research Center

Bing Ren From ChIP-chip to ChIP-Seq: unraveling the second code of the human genom

submitted by: dougramsey

Bing Ren From ChIP-chip to ChIP-Seq: unraveling the second code of the human genome presented by Bing Ren, University of California, San Diego

Illumina

submitted by: dougramsey
At Illumina, our goal is to apply innovative technologies and revolutionary assays to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. These studies will help make the realization of personalized medicine possible. With such rapid advances in technology taking place, it is mission critical to have solutions that are not only innovative, but flexible, scalable, and complete with industry-leading support and service. As...

Assembling Short and error-Prone DNA Reads

submitted by: dougramsey

Assembling Short and error-Prone DNA Reads presented by Pavel Pevzner, University of California, San Diego

Alta-Cyclic - A self Optimizing Base Caller for the Illumina Genome Analyzer

submitted by: dougramsey

Alta-Cyclic - A self Optimizing Base Caller for the Illumina Genome Analyzer presented by Yaniv Erlich, Cold Spring Harbor Labs