Seb Lunke Profile
Seb Lunke

@GenomeSeb

Followers
629
Following
2K
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65
Statuses
888

#Genomic #MedicalScientist, technophile, progress enthusiast. All views my own.

Melbourne, Victoria
Joined April 2016
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@GenomeSeb
Seb Lunke
10 months
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!.
@ZornitzaS
Prof Zornitza Stark
10 months
👉 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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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
RT @TJDaykin: Looking forward to the partnership between @MCRI_for_kids @TeamVCGS and @nanopore becoming prosperous for numerous patients.….
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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
RT @RareRevolutionM: #InternationalNeonatalScreeningDay: A call for global implementation of neonatal screening programmes. Read at https:….
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@GenomeSeb
Seb Lunke
1 year
RT @ZornitzaS: 👏👏👏Looking forward to working on this together @GenomeSeb @nanopore @TeamVCGS @MCRI_for_kids.
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@GenomeSeb
Seb Lunke
1 year
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.
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djsir.vic.gov.au
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@GenomeSeb
Seb Lunke
1 year
RT @TeamVCGS: Translating the outcomes of this project will be transformative for mainstreaming #genomics in Australian healthcare. Excitin….
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@GenomeSeb
Seb Lunke
1 year
RT @NatureMedicine: Exploring the benefits, harms and costs of genomic newborn screening for rare diseases. Comment from @ZornitzaS and co….
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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
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.
@dgmacarthur
Daniel MacArthur
1 year
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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@GenomeSeb
Seb Lunke
1 year
RT @dgmacarthur: The diagnosis of rare genetic disorders is one of the places where AI will have the earliest and largest clinical impact.….
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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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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
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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@GenomeSeb
Seb Lunke
1 year
RT @ZornitzaS: Starting now in A6/7 #eshg2024 Nonsense mediated mRNA decay: variant interpretation challenges with @GeczSquadGoals and @Gen….
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