--- title: Genomics in the Clinic & the Promise of Precision Medicine description: At PMLS Precision Medicine and Rare Disease event, Congenica took part in a panel entitled 'Genomics in the Clinic and the Promise of Precision Medicine'. image: https://blog.congenica.com/hubfs/Hear%20the%20panel%20session%20from%20PMLS%20Precision%20Medicine%20%26%20Rare%20Disease%20event.png --- - [Our Customers and Partners](http://www.congenica.com/our-customers) - [Our Product Portfolio](http://www.congenica.com/congenica-products) - **Inherited Diseases** - [Rare Disease](http://www.congenica.com/congenica-rare-disease) - [Inherited Cancer](http://www.congenica.com/congenica-inherited-cancer) - [Prenatal Health](http://www.congenica.com/congenica-prenatal) - [Carrier Screening](http://www.congenica.com/congenica-carrier-screening) - [Neurodevelopmental Disorders](http://www.congenica.com/congenica-neuro) - **Somatic Oncology** - [Solid Tumours](http://www.congenica.com/congenica-oncology) - **Pathogen** - [Pathogen Surveillance](http://www.congenica.com/congenica-pathogen-surveillance) - [Our Services](http://www.congenica.com/congenica-services) - [Clinical Interpretation Services](http://www.congenica.com/congenica-clinical-interpretation-services) - [Professional Services](http://www.congenica.com/professional-services) - [Customer Support](http://www.congenica.com/customer-support) - [Pharma Services](http://www.congenica.com/pharma-services) - Resources - [Publications](http://www.congenica.com/publications) - [Supporting materials](http://www.congenica.com/resources) - [News](https://blog.congenica.com/) - [Events and webinars](http://www.congenica.com/events-webinars) - [About us](http://www.congenica.com) - [Leadership Team](http://www.congenica.com/leadership) - [Quality](http://www.congenica.com/quality) - [Investors](http://www.congenica.com/investors) - [People and Vacancies](http://www.congenica.com/people) - [Contact us](http://www.congenica.com/contact) Login ##### Please select your location and reference genome: [America - GRCh37](https://us-37.congenica.com/) [America - GRCh38](https://us-38.congenica.com/) [Europe, Middle East, Africa - GRCh37](https://eu-37.congenica.com/) [Europe, Middle East, Africa - GRCh38](https://eu-38.congenica.com/) [Overview](https://blog.congenica.com) [Genomics in the Clinic & the Promise of Precision Medicine](https://blog.congenica.com/genomics-in-the-clinic-the-promise-of-precision-medicine) ![Genomics in the Clinic & the Promise of Precision Medicine](https://blog.congenica.com/hubfs/Hear%20the%20panel%20session%20from%20PMLS%20Precision%20Medicine%20%26%20Rare%20Disease%20event.png) Clinical Cases events precision medicine film rare diseases # Genomics in the Clinic & the Promise of Precision Medicine 6/22/2021    |    0 min read At the recent PMLS Precision Medicine Leaders’ Summit Virtual Series 2021 – Precision Medicine and Rare Disease, our Lead Clinical Scientist, Rare Disease, Andrea Haworth took part in a panel entitled: 'Genomics in the Clinic and the Promise of Precision Medicine'.   The panel of experts consisted of: - Chris Waters, CEO and founder of **Rare Science** (moderator) - Lynsey Chediak, Lead, Precision Medicine, Shaping the Future of Health and Healthcare, **World Economic Forum** - Chun-Hung Chan, PhD Director, Special Projects, **Sanford Research** - Andrea Haworth, Lead Clinical Scientist, Rare Disease, **Congenica** - Arthur Hermann, MS Strategic Technical Consultant, **Kaiser Permanente**   During the session, the panel shared their perspectives on the impact of early intervention using whole genome sequencing / whole exome sequencing and clinical decision support for diagnosis, based on their involvement in some of the world’s leading programs.   ## World-leading Congenica genomic analysis platform Find out how Congenica can help you to accurately interpret genomic data in minutes and reduce interpretation costs by 95%.   [![Discover Congenica ](https://no-cache.hubspot.com/cta/default/6863388/bb21528f-1dd0-45ce-86ba-bcfb072243bd.png)](https://cta-redirect.hubspot.com/cta/redirect/6863388/bb21528f-1dd0-45ce-86ba-bcfb072243bd)   --- ### Related articles ![Congenica and NoorDx deliver sample-to-report services across the Middle East](https://blog.congenica.com/hs-fs/hubfs/NoorDX%20announcement.png?width=320&height=192&name=NoorDX%20announcement.png) 6/22/2023 #### [Congenica and NoorDx deliver sample-to-report services across the Middle East](https://blog.congenica.com/congenica-noordx-deliver-sample-to-report-services-across-middleeast) Congenica announces a strategic partnership with NoorDx, an innovative clinical genomics and research services company in Saudi Arabia. ![The Real Costs of Rare Disease](https://blog.congenica.com/hs-fs/hubfs/Webinar%20the%20cost%20of%20rare%20disease%20(2).png?width=320&height=192&name=Webinar%20the%20cost%20of%20rare%20disease%20(2).png) 11/25/2022 #### [The Real Costs of Rare Disease](https://blog.congenica.com/the-real-costs-of-rare-disease) Congenica welcomed an expert panel to discuss the true cost of rare disease, from birth to diagnosis, childhood to adulthood. ![Reality Check of a 13th Birthday for a Caregiver](https://blog.congenica.com/hs-fs/hubfs/Reality%20Check%20of%20a%2013th%20Birthday%20for%20a%20Caregiver.png?width=320&height=192&name=Reality%20Check%20of%20a%2013th%20Birthday%20for%20a%20Caregiver.png) 7/28/2022 #### [Reality Check of a 13th Birthday for a Caregiver](https://blog.congenica.com/reality-check-of-a-13th-birthday) As part of our mental health initiative, Nicole Duaz talks about being mother to Summer, who has a rare genetic disease and autism, and a self-care coach. ##### Congenica is available as a CE Marked IVD clinical decision support platform for clinical diagnostic use for inherited genetic disorders in the UK and EU, Iceland, Lichtenstein, Norway, Switzerland and Turkey. In all other countries, ensuring compliance with relevant local, national and international clinical laboratory regulations is the responsibility of the laboratory. - [Privacy Policy](http://www.congenica.com/privacy-policy) - [Cookie Policy](http://www.congenica.com/cookie-policy) Log in to Congenica ##### Please select your location and reference genome: [America - GRCh37](https://us-37.congenica.com/) [America - GRCh38](https://us-38.congenica.com/) [Europe, Middle East, Africa - GRCh37](https://eu-37.congenica.com/) [Europe, Middle East, Africa - GRCh38](https://eu-38.congenica.com/) ![CE](https://blog.congenica.com/hs-fs/hubfs/CE.png?width=80&height=80&name=CE.png) ![ISO-27001](https://blog.congenica.com/hs-fs/hubfs/ISO-27001.jpg?width=80&height=80&name=ISO-27001.jpg) ![TR-Testmark_9000030872_EN_2024_CMYK](https://blog.congenica.com/hs-fs/hubfs/2023%20website%20images/TR-Testmark_9000030872_EN_2024_CMYK.png?width=80&height=80&name=TR-Testmark_9000030872_EN_2024_CMYK.png) ![HIPAA Compliant](https://blog.congenica.com/hs-fs/hubfs/HIPAA%20Compliant.png?width=80&height=80&name=HIPAA%20Compliant.png) Copyright © 2026 Congenica Ltd. Company number: 8273616 Registered in England and Wales. ```json { "@context" : "https://schema.org", "@type" : "VideoObject", "contentUrl" : "https://6863388.fs1.hubspotusercontent-na1.net/hubfs/6863388/Genomics%20in%20the%20Clinic.mp4", "dateModified" : "2022-05-27T03:50:43.257Z", "description" : "Congenica's Lead Clinical Scientist, Rare Disease, Andrea Haworth, joins experts from RARE Science, Sanford BioBank, World Economic Forum and Kaiser Permanente for a panel session at PMLS Virtual Series 2021 – Precision Medicine & Rare Disease event. During the session 'Genomics in the Clinic and the Promise of Precision Medicine', the panel's experts share their perspectives on the impact of early intervention using WGS/WES and clinical decision support for diagnosis, based on their involvement in some of the world’s leading programs.", "duration" : "PT59M8S", "height" : 720, "name" : "Genomics in the Clinic and the Promise of Precision Medicine", "thumbnailUrl" : "https://api-na1.hubapi.com/filemanager/api/v3/files/thumbnail-redirect/48983989606?portalId=6863388&size=medium", "uploadDate" : "2021-06-17T13:36:41.146Z", "width" : 1280 } ```