GenomeSeb
@genomeseb.bsky.social
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#Genomic
#MedicalScientist
, technophile, progress enthusiast. All views my own.
reposted by
GenomeSeb
Dr Monique Ryan
about 1 month ago
The government can’t claim that medical research is a priority while failing to treat it as one. Nine in 10 leading researchers in Australia are missing out on government support for world‑class proposals, leaving exceptional talent uncertain about their future.
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Most researchers miss out on innovation grants while medical fund sits on $25b
Nine in 10 Australian researchers had their “ideas grant” applications rejected last year, even as Australia’s medical investment fund sits on $5 billion more than it was designed to hold.
https://www.theage.com.au/politics/federal/most-researchers-miss-out-on-innovation-grants-while-medical-fund-sits-on-25b-20251230-p5nqp9.html
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reposted by
GenomeSeb
Zornitza Stark
30 days ago
Genomic Newborn Screening: Commodity or Public Good?
onlinelibrary.wiley.com/doi/10.5694/...
What's next for genomic NBS in Australia? Commercial testing? Publicly funded program? Large scale research to build capacity, infrastructure and evidence? We discuss the options & ethics ⚖️
@mja.com.au
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Genomic Newborn Screening: Commodity or Public Good?
Genomic newborn screening (gNBS) can screen for a broad range of genetic conditions, potentially enabling early treatment and improving health outcomes. However, it remains outside publicly funded pr...
https://onlinelibrary.wiley.com/doi/10.5694/mja2.70135
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reposted by
GenomeSeb
Zornitza Stark
4 months ago
🤗 Out now
@naturemedicine.bsky.social
results of our genomic NBS study BabyScreen+ 👶🧬 👉
www.nature.com/articles/s41...
1,000 babies WGS using existing cards 600+ conditions 13 day TAT 16 diagnoses (vs 1 in std NBS) High clinical impact High parental acceptability
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Proud to share our BabyScreen+
#gNBS
study is now out in
@naturemedicine.bsky.social
: 1000 babies screened, results in <2wks, 16 high chance findings, incl. 2 with major impact on care. Big thanks to
@zornitza.bsky.social
and the study team!
www.nature.com/articles/s41...
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Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study - Nature Medicine
The BabyScreen+ study offered genomic screening to 1,000 newborns in Australia, and showed that the approach is feasible and positively received by families, leading to molecular diagnoses in 1.6% of babies.
https://www.nature.com/articles/s41591-025-03986-z
4 months ago
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reposted by
GenomeSeb
Caroline Wright
9 months ago
Pretty excited about giving Talos a try in the NHS
@rdexeter.bsky.social
. We should definitely be doing regular reanalysis of existing genome-wide sequencing data, just need the right tools!
add a skeleton here at some point
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reposted by
GenomeSeb
Zornitza Stark
9 months ago
What does the Australian public think about the value and implementation of genomic NBS? 🧬👶⚖️
@ajhgnews.bsky.social
@iliasgoranitis.bsky.social
@stephaniebest.bsky.social
@genomeseb.bsky.social
@genetic-fi.bsky.social
#raredisease
#genomics
#healtheconomics
www.sciencedirect.com/science/arti...
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Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia
Integrating genomic sequencing into newborn screening (NBS) has transformative potential for the identification and management of genetic conditions. …
https://www.sciencedirect.com/science/article/pii/S0002929725001818
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Already so many benefits, and this is only just the start for Talos!
add a skeleton here at some point
9 months ago
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@zornitza.bsky.social
updating on Talos automated reanalysis pipeline
#ESHG2025
>250 new diagnosis from 4744 unsolved cases. That’s 5% new extra for <1 variant per case, it’s
#scaleable
! Pre-print now out:
www.medrxiv.org/content/10.1...
Talos is
#portable
#opensource
:
github.com/populationge...
9 months ago
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reposted by
GenomeSeb
R-Synapse
9 months ago
Daniella Hock, U Melbourne: proteomics diagnostics in rare disease. Fascinating ECHS1
#epilepsy
synonymous + del compound heterozygous variant w/ founder effect/regional polymorphism. Rapid proteomics testing ~$1.000, cave(!) fibroblast/tissue cultivation time.
#eshg2025
#genetics
#proteomics
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reposted by
GenomeSeb
European Society of Human Genetics
9 months ago
🌟 Trainees & Recruiters! 🌟 Don't miss the
#ESHG2025
MatchMaking! Whether you're ready to take the next step in your career or seeking fresh talent, join us today at the
#ESHG-Y
booth 546 in Hall 4 at 12:00 hrs CEST. Let's connect and advance our careers in
#genetics
together!
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Thank you
@ahoischen.bsky.social
and Lot Snijders Blok for hosting the Poster lightalk session. It was indeed a lot of fun, and a lot of great work presented.
#ESHG2025
9 months ago
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reposted by
GenomeSeb
Zornitza Stark
9 months ago
Too much great stuff on this morning
#ESHG2025
, on at sequencing square: lightening poster talks!
@genomeseb.bsky.social
now presenting results from the BabyScreen+ study
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Should be an exciting session this morning in Brown 3
#Eshg2025
discussing the latest in genomic newborn screening. Kicking off is the amazing
@zornitza.bsky.social
with an interactive hot topic session on what conditions to include.
9 months ago
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reposted by
GenomeSeb
James Fasham
9 months ago
🗣️ Quote of
#ESHG2025
(so far) "Who licks bone !?!" 🦴 - Johannes Krause Anyone have that on your bingo card? Well apparently archeologists do, to distinguish bone from stones and it causes problems in DNA sequencing. 🤔
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reposted by
GenomeSeb
Tim Frayling
9 months ago
Steve McCarroll plenary. Amazing to go back to Huntington's disease, and learn there is nothing toxic about inherited CAG expansion, its their random somatic expansion over a relatively short period of time. Explains a lot about later onset of condition.
#ESHG2025
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reposted by
GenomeSeb
James Fasham
9 months ago
Release announcement from T2T consortium!
humanpangenome.org/hprc-data-re...
#ESHG2025
. Combining @nanopore @pacbio and @illumina data to improve the T2T pangenome 🧬
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HPRC Data Release 2
HPRC Data Release 2
https://humanpangenome.org/hprc-data-release-2/
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reposted by
GenomeSeb
European Society of Human Genetics
9 months ago
Attend the ELPAG Award lecture at 14:15 at
#eshg2025
with Sylvia Metcalfe who played a leading role in setting up the Genioz project and find out about her research that led to the ELPAG Award.
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reposted by
GenomeSeb
Alex Hoischen
9 months ago
Getting ready for
#eshg2025
…and our postdoc
@lydiasagath.bsky.social
made a nice BINGO card again. Paying a lot of attention to the entire event will pay off!
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reposted by
GenomeSeb
Zornitza Stark
9 months ago
And we’re off
#ESHG2025
! Now on implementing
#genomics
at scale: Lil Downie talking about our experience of using digital decision support on genomic NBS
@genomeseb.bsky.social
@yvonnebombard.bsky.social
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This is great work showing how regular automated re-analysis of genomic data for negative cases yields new diagnosis in a scalable way. No AI required!
add a skeleton here at some point
9 months ago
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reposted by
GenomeSeb
Zornitza Stark
about 1 year ago
📣 Out now in
#HumanGenomics
! 🤔 What do the public think about the use of AI in
#genomic
medicine? 👉
rdcu.be/d0PLP
Benefits: efficiency ⬆️ errors ⬇️ Concerns: data security 🔐 discrimination Who would be liable for error? 🤖👩⚕️
@genetic-fi.bsky.social
Danya Vears & Jack Harrison 👏
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Analysis of public perceptions on the use of artificial intelligence in genomic medicine | Human Genomics
https://rdcu.be/d0PLP
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