BioCurious Message Board › Consensus structure variant calling, HugeSeq, workshop on Jan 22, 2014
I wanted to announce that one of Stanford developed pipelines for variant analysis is now available to larger genomics community via Seven Bridges Cloud platform. They have arranged for a workshop where you can learn more and try it out.
Please visit our homepage > TWEETS section to learn more.
Director Big Data Genomics Core
Stanford School of Medicine