The IMPC at Genomics of Rare Disease

The IMPC is excited to be attending the Genomics of Rare Disease meeting, starting this week on Wednesday 27th March at the Wellcome Genome Campus Conference Centre, UK. The programme features the latest research related to the genomic basis of rare disease and will focus on key areas such as informatics, developmental genetics and functional genomics.

We are looking forward to engaging with scientists, students and clinicians to raise awareness of the IMPC as a resource. If you are attending the conference and want to learn more about the IMPC and how we can benefit you in your research, please visit our stand in the exhibition area where we will be happy to talk to you about the work that we do.

We will be tweeting throughout the meeting so please follow us on Twitter for updates or keep up to date with Genomics of Rare Disease at #GRD19

The IMPC

The International Mouse Phenotyping Consortium (IMPC) is a global effort to identify the function of every protein-coding gene in the mouse genome. This growing catalogue of mammalian gene function is freely available for researchers. For more information, please click here.

Read about how IMPC data has been used in recent research:

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