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Rare Inherited Disease: 30 Min from data to report

This is a recording of a webinar hosted on March 7th 2017. In this webinar, you will learn how Congenica can help clinical geneticists reach a faster and more accurate diagnosis for patients presenting with phenotypes of a rare inherited disease.
Andrea Haworth, Head of Clinical Services at Congenica and Laura Reed, Pre-Registered Clinical Scientist at Congenica share their experiences of Whole Genome Analysis and the insights gained from using the Congenica platform with the Genomics England 100K Genomes Project.
Challenges and Tribulations of Whole Genome Variant Interpretation
Andrea Haworth: Head of Clinical at Congenica
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