Training

Next generation sequencing is the ultimate tool for all varieties of genetic studies including metagenomics and population studies, epigenetics, transcriptomics, health and disease genetics, genome de novo assembling and re-sequencing. Combining the world's resource of next generation data into one publicly accessible place maximises the potential for finding patterns and comparing like datasets. This is the ultimate dataset for bioinformatics tools and it resides in EBI's Sequence Read Archive (SRA).

During the workshop we will talk about how to represent your own experiments and how to extract the datasets that you need for your analysis interests.

This session will usually be offered as one of a number of short introductions to EBI Services that can be booked separately.