Last chance to register for the AFGN Symposium and take advantage of early bird pricing!
📢Register by COB tomorrow: Friday, Oct 25.
Secure your ticket here: https://t.co/y7TrnuqxVo
📢 EOI open for funding (up to $200K) to establish platforms to assess VUS in priority genes.
🧬Review the high-priority gene list and register your interest: https://t.co/27S7aXVjXz
📩Submit by Oct 4th
#Genomics#ResearchFunding#AFGN
Registrations and abstract submissions for the 2024 AFGN Symposium are open!
Join us on November 28 & 29 in Melbourne.
📢Abstract submissions close: Sept 13th
🎟️Early bird registration closes: Oct 25th
Learn more: https://t.co/pE3ZKnT4ku
#RareDisease#FunctionalGenomics
Attention all FxGx researchers ! ⚠️ Time is running out to apply for our latest funding round to help tackle VUS in priority genes. ⏰ Less than a week left to submit your application! Let's work together to make a difference. Applications close March 27th https://t.co/tOfH0lFzwe
Australian Functional Genomics Network (AFGN) announces a new funding for functional genomics platforms to resolve multiple VUS in priority genes. Projects will be eligible for catalyst funding up to $200,000. Applications close March 27th. APPLY NOW. https://t.co/Czu8bOGa47
If you have any questions/would like to know more about Pipeline Accelerator, join our virtual information session which will be held on the 14th of March 2023, 12pm AEST.
https://t.co/ayEbQSQfQ9
Healthcare professionals, help your unresolved genetic testing patients by connecting with research teams! Our program provides funding for functional validation of genomic findings. Apply now! https://t.co/k0ZCzAJyGP #genomicsresearch#functionalvalidation#medicalresearch
New funding opportunity for FxGx researchers! Apply for catalyst funding up to $200k to develop platforms to resolve multiple VUS in priority genes for Australian labs & clinicians. Apply now: https://t.co/WbalxxANWz #functionalgenomics#researchfunding#VUSresolutions
Pipeline Accelerator 2022-23 Round 2 will open for applications next Monday. In partnership with
@TIA_Aust, we collectively offer you access to a
range of translational medical research capabilities. Join our info session 14 Mar 12pm AEST for more info
https://t.co/FctQS09P3z
The impact of Australia’s national initiative to accelerate the use of #genomics in mainstream healthcare has been captured in a report published in @AJHGNews.
👉 https://t.co/EqbRs8OVW8
Excited to present new genomics tool: we use complex trait genetic data to study organisation of cellular gene programs. We then use it to predict genetic causes of disease from underpowered gwas. Great work from @DaliaMizikovsky. https://t.co/oAOtMNBREq
Scientists in the Telomere-to-Telomere (#T2T) consortium have published the first complete, gapless human genome sequence. This can lead to a better understanding of our genomic variations and provide insight for missing heritability and human disease. https://t.co/zZBpKbDKHd
Help us grow our researcher registry !!
We are calling all model organism researchers to join our registry for the opportunity to receive funding for patient-driven research.
Follow the link to sign-up 👇
https://t.co/8lAkGOcmja
#Genomics#research