At Unique, we know only too well how gathering information from families can help to improve our understanding of rare chromosome and gene disorders.

We recently shared details of a webinar held by Genomics England about the 100,000 Genomes Project highlighting the impact of participant data so far and answering questions from participants on how science and tech are evolving and their approach to analysis. Click here to read a highlights blog and find a list of the Q&As.

You can view a recording of the webinar here: