Webinar: Re-analyse RNA-Seq public data from SRA
Dr. Pablo Prieto explains the fundamentals of re-analysing RNA-Seq public data from Sequence Read Archive (SRA) and discusses some common questions and issues that arise from these analyses.
Over the last few years open-source has been increasingly becoming the norm, even in Bioinformatics. The number of high-quality applications which are freely available on GitHub and other Git providers is increasing, such as the pipelines that the Broad institute uses for production.
In December 2017, the team at Google Brain joined the effort by releasing an open source, deep learning based variant caller: DeepVariant. DeepVariant outperforms its competitors by accuracy – it even won the accuracy award at the precision FDA Truth Challenge.