With support from Invest Victoria, Illumina & University of Melbourne established TAGC—presenting an opportunity to transform patient outcomes and create substantial efficiencies for the healthcare system through #genomics-driven personalised care. Read & watch more: invest.vic.gov.au/resources/case…

I’m incredibly excited that President Barack Obama will attend the @Illumina #Genomics Forum this fall to discuss the need for increased health care equity and smarter healthcare to improve the human condition.

Innovation to say the least!!! What a cool initiative #Genomics #illumina #marineconservation

Has any club treated their fans worse in the last decade than #Essendon …. Doubt it #AFL #clarko

That tribunal appeal proved worthwhile in the end.

This was a lot of fun to make! We filmed it just before COVID hit and so paused its release. We'll be releasing more short versions in the coming months, but do check out the long version. Feel free to use it in explainers for students or lay audiences youtube.com/watch?v=-nty4s…

The Australian Acute Care Genomics program report shows that integrating rapid whole genome sequencing and multiomic analyses informs diagnoses and treatment decisions in a prospective cohort of 290 critically ill infants & children. Prof Zornitza Stark Seb Lunke nature.com/articles/s4159…

Turn it up mate, I get that you’re just regurgitating the rule book but right now you’re reminiscent of the yuppie ponytail that Matt Damon schools in Good Will Hunting…of course that’s your contention!

Spine tingling stuff

A landmark study in the UK has revealed widespread genetic variations that were common across some of the most deadly cancers: bit.ly/4aQPbJk

Dr Dr Jane Tiller explains how the impact of not being able to get life insurance is stopping Australians from getting genetic testing, and what changes need to happen to the system.

Hot off the press: Our BabyScreen+ list of over 600 actionable genes and conditions that we screen for in our #gNBS pilot now published: gimjournal.org/article/S1098-… Thanks to the great work of Prof Zornitza Stark, Lilian Downie and many others.

Attending Lorne Cancer Conference this week? Come along to hear from Martin Smith and Robert Day as they share their cutting edge cancer research using Nanopore Sequencing. Register at the link below. nanoporetech.com/about/events/c… #LorneCancer2024 #WYMM

🤗 Absolutely thrilled to see our #AcuteCare ⁦Australian Genomics⁩ work featured ⁦nature⁩ together with ⁦ExeterGenomes⁩ ⁦Rady Genomics⁩ ⁦euan ashley⁩ 🧬⏱️🤗 nature.com/articles/d4158…

Standing room only at the first stop of the ANZ #WYMM tour Oxford Nanopore

Excited to receive VMRAF 💰 by Victorian Government @VicGov_DJSIR to pilot Oxford Nanopore to detect repeat expansion disorders! This will enable us to substantially improve #genetic #diagnosis for many #neurological conditions. djsir.vic.gov.au/medical-resear… Murdoch Children's Research Institute (MCRI) Victorian Clinical Genetics Services (VCGS)

Kudos to the team at Victorian Clinical Genetics Services (VCGS) and the Murdoch Children's Research Institute (MCRI) a groundbreaking approach using Oxford Nanopore to drastically improve diagnosis of RE disorders and deliver significant healthcare benefits

Looking forward to the partnership between Murdoch Children's Research Institute (MCRI) Victorian Clinical Genetics Services (VCGS) and Oxford Nanopore becoming prosperous for numerous patients. Innovative times ahead!! Seb Lunke #RareDisease #genetics

Unlock the power of Oxford Nanopore Technologies. ⁦Victorian Clinical Genetics Services (VCGS)⁩ now offers cutting edge long read sequencing for research!! Get started with ⁦⁦Oxford Nanopore⁩ sequencing today #ONT #longreads vcgs.org.au/long-read-sequ…

It was so interesting to see a lot of clinical labs using Oxford Nanopore . The slide from Morghan Lucas, MGZ summarizes the added value they get from ONT in the case of FSHD