Analysis of Copy Number and Structural Variants in Whole-Genome Sequencing Data.Thursday, 19 April 2012 at 17:00 Add to Calendar ▼2012-04-19 17:00:002012-04-19 18:00:00Europe/LondonAnalysis of Copy Number and Structural Variants in Whole-Genome Sequencing Data.SELECTBIOenquiries@selectbiosciences.com Recent advances in NGS allow high-coverage sequencing of the human genome at an affordable cost. We will describe computational methods for analysis of DNA copy number and structural variation, as well as their applications to detection of somatic variants in cancer genomes. |