Australian Functional Genomics Network
@AFGNetwork
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"Match-making" clinicians and model organism researchers to improve understanding of the genetic basis of rare disease.
Joined March 2022
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
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📢 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
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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
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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
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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
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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
Applications for Pipeline Accelerator 2022-23 Round 2 is now open. In this Pipeline Accelerator round, we are partnering with @TIA_Aust to expand the portfolio of services and expertise enabling medical research discovery and translation. For more info https://t.co/oLaPjNHdgc
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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
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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
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Another great funding resource for disease modelling !!
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
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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
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Hope to see everyone at ComBio in Melbourne, include Genetics Society of AustralAsia for the first time. Will be a great meeting! Please retweet @GeneticsAus @Genetics2023 @LIMSLTU @Monash_Science @BioSci_UniMelb @MonashBDI @MonashBiol @ResearchMenzies @UTAS_MedSci
We are excited to announce that you can now register and submit your abstract for #ComBio2022 🥳 Early registration and abstract deadline is June 24. Look forward to seeing you *face-to-face* soon 🙌🏼 https://t.co/f1yCLX1bML
@ITSASBMB @asps_ozplants
@ANZSCDB @GeneticsAus @nzsbmb
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Clinical applications are now open for @AFGNetwork. Fill out the submission survey to propose your patient(s) variant(s) for functional studies 👉👉 https://t.co/00GqDFkyVt
@n_palpant @KerryDozheart @gemtreee
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Our #RDMM partner network @modelmatchernet published their platform #ModelMatcher facilitating collaborations between stakeholders of #RareDisease and #undiagnosed disease research. @AFGNetwork @micyrn @NIG_idenken
New publication from our colleagues @BaylorGenetics describes #ModelMatcher, "a global online matchmaking tool designed to facilitate cross-disciplinary collaborations." https://t.co/xWk0ubjCHP
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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.
biorxiv.org
Genome wide association studies provide statistical measures of gene-trait associations that reveal how genetic variation influences phenotypes. This study develops an unsupervised dimensionality...
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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
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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
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Welcome to #Twitter @AFGNetwork: watch this space, exciting things to come, we are almost ready to roll!! 🤗🤗🤗 @AusGenomics @kidgenaustralia @GeczSquadGoals @scott_lab_gmp @monashdevneph @emmagenetics @ChiragVPatel79 @CoralWarr @RobertB_R @n_palpant @EbonyMatotek
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