Great new tool

Ever since I've heard of the existence of the NGS logistics tool, I've been using it quite frequently. It is a great tool to investigate local exomes, since most of the available data on public databases, although from European origin, is not always very closely related to our Belgian population. For my project we investigate rare variants, so ancestry is very important in our project. One downside is that although you can see the frequency of the variant, you cannot immediately see if it is present in unrelated or related individuals, which can bias your result. However, since you receive the patient ID, you can always go back to the collaborator who presented the data to check these kind of things