
Seb Lunke
@GenomeSeb
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#Genomic #MedicalScientist, technophile, progress enthusiast. All views my own.
Melbourne, Victoria
Joined April 2016
This 👇👇👇!!! I think data sharing is an absolute must, and can be done in a way that ensures privacy and patient autonomy while providing huge benefits to individuals, research and society. Even a small start is a start, let’s break down the silos. Please do!.
👉 Out now @NatureRevGenet: we CAN and we SHOULD do more to enable #genomic data sharing! 🧬🌏. 👉Best practice examples and 12 actions we can all take together. 👉 @GA4GH @AusGenomics @GenomicsEngland @NHSgms @AllofUsResearch @uk_biobank @ukfuturehealth
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RT @AusGenomics: New publications from @AusGenomics & @MCRI_for_kids in @AJHGNews led by A/Prof Amy Nisselle & @bronwynterrill aim to impro….
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RT @TJDaykin: Looking forward to the partnership between @MCRI_for_kids @TeamVCGS and @nanopore becoming prosperous for numerous patients.….
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RT @MCRI_for_kids: Congrats to #MCRI's A/Prof Sebastian Lunke who has received a Victorian Medical Research Acceleration Fund grant to deve….
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RT @rossnapoli86: The most exciting part for me will be seeing how this work will improve the lives of those suffering from hard to diagnos….
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RT @RareRevolutionM: #InternationalNeonatalScreeningDay: A call for global implementation of neonatal screening programmes. Read at https:….
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RT @ZornitzaS: 👏👏👏Looking forward to working on this together @GenomeSeb @nanopore @TeamVCGS @MCRI_for_kids.
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Excited to receive VMRAF đź’° by @VicGovAu @VicGov_DJSIR to pilot @nanopore to detect repeat expansion disorders! This will enable us to substantially improve #genetic #diagnosis for many #neurological conditions. @MCRI_for_kids @TeamVCGS.
djsir.vic.gov.au
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RT @NatureMedicine: Exploring the benefits, harms and costs of genomic newborn screening for rare diseases. Comment from @ZornitzaS and co….
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RT @dgmacarthur: @ZornitzaS @TeamVCGS @MCRI_for_kids Stoked that we get to extend our already hyper-productive work together in a whole bun….
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RT @ZornitzaS: Sooooo excited to be doing this with you @dgmacarthur and building on the 💪 collaborations we have established in automation….
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Exited to be part of this new initiative! The promises of AI are many fold, this project will help us harness them the right way to help more people with rare genetic diseases.
The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact. Delighted to be leading a new consortium to help make this happen, along with an awesome team of Australian and global partners:
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RT @dgmacarthur: The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact.….
mcri.edu.au
A consortium of Australian and international partners that aims to leverage advances in AI technology will be created after funding was awarded. Read more.
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RT @ZornitzaS: 📣 our latest BabyScreen+ paper now out @ejhg_journal . Process changes needed to deliver #genomic NBS: what, when and who?….
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RT @ZornitzaS: Out now @NatureMedicine 🔥🔥. #genomic NBS: the challenges are daunting . But we have a responsibility to lead research in pub….
nature.com
Nature Medicine - The prospect of genomic screening in newborns attracts both hype and criticism, but carefully designed, large-scale, prospective research studies are the only way to generate the...
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RT @IliasGoranitis: In a new paper published in @NatureMedicine, we show that @EmotiveTrial early detection & bundled treatment of #postpar….
nature.com
Nature Medicine - An economic evaluation of the E-MOTIVE intervention for postpartum hemorrhage (PPH) compared with usual care in 210,132 women, carried out from a healthcare system perspective,...
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RT @ZornitzaS: On now in A3, the new gene 🧬 discovery of the year: RNU4-2 is a frequent cause of DD/ID. A fantastic, whirlwind collaboratio….
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RT @ZornitzaS: Starting now in A6/7 #eshg2024 Nonsense mediated mRNA decay: variant interpretation challenges with @GeczSquadGoals and @Gen….
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