The Participant Panel are recruiting for a new Chair and members. The Panel plays a vital role in keeping participants’ interests at the heart of everything Genomics England does. Get in touch to apply and help champion participants’ interests. Applications for the Chair role close 30 September, and applications for member roles close 11 October. https://ow.ly/syPt50SS8xh
Genomics England
Biotechnology Research
We’re working to enable faster and deeper genomic diagnosis & research, to bring genomic healthcare to all who need it.
About us
Genomics England works with the NHS to bring forward the use of genomic healthcare and research in Britain to help people live longer, healthier lives. Genomics is a ground-breaking area of medicine that uses our unique genetic code to help diagnose, treat and prevent illnesses. Thanks to advanced technology, scientists can now compare many people’s genetic code to make new discoveries that continually improve genomic healthcare. In 2013, Genomics England and the NHS launched the 100,000 Genomes Project, demonstrating how genomics insights can help doctors across the NHS, and building a foundation for the future by assembling a unique dataset. Genomics England is now supporting the NHS to deliver genomic testing for patients as part of routine healthcare, and providing the health data and technology that researchers need to make new discoveries and create more effective, targeted medicines. We work with thousands of people – patients, doctors and scientists – to increase our collective knowledge and enable faster and deeper genomic research, to bring genomic healthcare to all who need it.
- Website
-
http://www.genomicsengland.co.uk
External link for Genomics England
- Industry
- Biotechnology Research
- Company size
- 201-500 employees
- Headquarters
- London
- Type
- Government Agency
- Founded
- 2013
- Specialties
- Genomics, Next Generation Sequencing, Health Services, Bioinformatics, Whole Genome Sequencing, Data science, Oncology, Rare diseases, Diagnostics, Genomic healthcare, Healthcare, Clinical data, Real world evidence, and Diagnostics
Locations
-
Primary
1 Canada Square
London, E14 5AB, GB
Employees at Genomics England
-
Jon Lenihan
Project Management | Program Management | Delivery | Stakeholder Management | Mobile App Delivery | Software | Healthcare | Telecommunications |…
-
Gordana Mutadich
-
Peter Sinden
CIO @ Genomics England | Leading Big Data Analytics Initiatives and Cloud
-
Rachel Andre
Principal Content Designer
Updates
-
Next week our podcast guests discuss the importance of engaging people with lived experience of sickle cell in research and advocacy. Look out for the episode, live on Wednesday 🎙️ #SickleCellAwareness
-
We were delighted to host Cancer52 member organisations in our offices today. An opportunity for insightful conversations on how to maximise the impact of genomics in rare conditions and cancer through collaboration.
Delighted to be part of today’s roundtable event hosted by Genomics England, alongside Cancer52 charity member organisations. We’re here to explore collaborative opportunities and look into how whole genome sequencing (WGS) data can be used to maximise the impact of genomics for rare and less common cancers patients - to benefit from early detection, accessing best treatments, and contributing to research for improved future treatment options. #cancer #genomics #rarecancer #cancerresearch #cancercharity #collaboration
-
This month's Research Environment Training Session will look at how to use to use data held by Genomics England for publications and reports. Register to join fellow Research Network or Discovery forum members on 10 September 1.30 - 3pm via this link: https://ow.ly/aLzh50Tcp7t
-
Despite the genetic cause for sickle cell being known for decades, there is still a limited understanding of the mechanisms behind wide variability in disease progression. Therefore, currently there is an increased interest in generating genomic data on sickle cell. Genomics England, in collaboration with Sickle Cell Society and the James Lind Alliance are working towards outlining priority areas for patients and healthcare professionals through a priority setting partnership. To find out more, revisit our podcast from World Sickle Cell Day 2023: https://ow.ly/x3pX50Tcp1X
-
September marks Sickle Cell Awareness Month, join us in raising awareness and support for those living with sickle cell. Throughout the month, we will be sharing content and resources to help spread knowledge and understanding, so be sure to follow our socials for updates! To find out more about what sickle cell is, visit: https://lnkd.in/gDAgaCP #SickleCellAwareness Sickle Cell Society
-
An exciting opportunity that may be of interest for those researchers in our Pan-Cancer and Molecular Oncology Community. This free residential event, taking place from 25-28 November 2024 is being led by Cancer Research UK, in partnership with the MRC National Mouse Genetics Network, to collaborate with and compete against multidisciplinary teams of data and cancer experts at their first Spatial Biology Data Challenge. Find out more below, and apply by 16 September via this link: https://bit.ly/3Mi7pZj
Applications for our first Spatial Biology Data Challenge, in partnership with MRC National Mouse Genetics Network, are now open! We’re inviting multidisciplinary data and cancer experts to join our data challenge and use large-scale spatial biology data to further cancer research. You’ll need to leverage the diverse experience within your group to create or develop tools for earlier cancer detection and prevention. This free residential event will take place on 25-28 November 2024 at Mercure Glasgow City Hotel, Scotland. Domestic travel, accommodation and meal costs will be covered. Find out more about the challenges and who we’re looking for. Apply by 16 September 👉 https://bit.ly/3Mi7pZj #CRUKDataChallenge
-
How can we solve the challenges of multimodal data? This blog talks through the expansion of our cloud-based Research Environment and the open-source codebases we have developed to accelerate research on multimodal datasets. Read more in the latest technical blog, linked below. https://ow.ly/w2W550T9uR2
-
Dave was born with limited vision in his left eye, and was later diagnosed with microphthalmia, a rare eye condition. Find out more about the condition, as well as Dave’s work helping patients and participants, via this link: https://ow.ly/BFwg50SNhz4
-
New episode of Behind the Genes out now! In this episode, we discuss the barriers that diverse communities face in accessing genomic healthcare. Our guests explore how language barriers, cultural differences and socioeconomic factors impact acceptance and access to genomic medicine among marginalised communities. They also highlight the importance of educating healthcare professionals to communicate in culturally sensitive ways, and strategies that have been effective in fostering trust and engaging communities in genomic research and healthcare initiatives. Listen via this link: https://ow.ly/y41i50T8nUZ Moestak Hussein Aman Ali Rareminds