Neil Ward
@GenomicsUK
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Improving the health of the planet with genomics. VP and General Manager for PacBio EMEA.
United Kingdom
Joined February 2014
Congratulations to all the #HiFiSolves consortium on their latest paper:HiFi sequencing accurately identifies clinically relevant variants in paralogous genes
medrxiv.org
Short-read sequencing (SRS) methods have improved the detection of small genetic variants but remain limited in highly homologous genomic regions, such as segmental duplications with gene-pseudogene...
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After an evaluation of various technologies, long-read whole-genome sequencing is at present the only reliable approach to confirm the absence of foreign DNA in genome-edited crops https://t.co/fh2YHQhTXr
https://t.co/GU8slKhBXS
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Today in @Bloomberg, I discuss how advances in genomic sequencing are changing what’s possible for inherited diseases like Huntington’s – offering hope to families and a path towards potential cures. Read the interview here.👉 https://t.co/5mB6txwD6N #Genomics
bloomberg.com
Hi, this is Naomi in Berlin. Today I’m looking west to Scotland, where the possibility of a treatment is inspiring some people to test for a devastating genetic disease. More on that in a moment, but...
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In the latest edition of @LaboratoryNews, I explore the diversity problem in genomics and delve into PacBio’s work on the first Arab pangenome. Read more here👉 https://t.co/S5UYugXQQD
#Genomics #diversity
cloud.3dissue.com
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Today in @Labiotech.eu, I discuss the global impact of rare diseases, the factors behind regional prevalence, and how long-read sequencing is driving new insights into disease mechanisms. Read the full article here.👉 https://t.co/4QrgcVLVyk #Genomics
labiotech.eu
Learn why rare diseases are more common in some communities due to cousin marriages and founder effects in population genetics.
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Today with @AZoLifeSciences, I explore the UK’s newborn sequencing programme and why long-read sequencing could be a game-changer in this evolving landscape. Read more:
azolifesciences.com
We spoke with Neil Ward from PacBio about England’s plan to introduce whole genome sequencing for every newborn, and how long-read technology is shaping the future of early diagnosis around the world.
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Is it just me that is a little disappointed that the UK government’s strategy docs can’t even get the number of bases in the double helix correct? Is this a sign of what happens when you rely too much on AI? #Genomics
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In @pathologistmag, I discuss how genomic sequencing of zoonotic pathogens is key to preventing future pandemics. Discover how long-read sequencing is transforming biosurveillance and understanding of zoonotic threats: https://t.co/xCr9ANJPcg #Genomics #PandemicPreparedness
thepathologist.com
Why we must urgently boost biosurveillance for zoonotic pathogens
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In @MoneyWeek, I discuss how Estonia’s National Biobank is turning genetic data into a powerful tool for personalised medicine. From disease prediction to tailored treatments, biobanks are reshaping healthcare as we know it. Read more here.👉 https://t.co/qebeFOcF6m
#Genomics
moneyweek.com
Developments in genomics are enabling the rise of personalised medicine, with therapies tailored specifically for individuals. Smart investors should buy in now, says Matthew Partridge
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In @Medicine_maker, I explore how advances in #longread sequencing are helping decode the dark regions of the genome.🧬 The latest generation of long-reads are accelerating research into pharmacogenomics, rare diseases, and cancer. Read more here: 👉
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In @DDWJournal, I share my prediction for rare disease research in 2025. With advances in long-read sequencing, researchers can unlock the ‘dark regions’ of the genome and identify the genetic underpinnings of rare diseases. Read more here.👉 https://t.co/Ukbkux33Xm
#Genomics
ddw-online.com
DDW spoke with industry experts about their predictions for drug discovery opportunities in 2025 for new modalities in drug discovery.
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To celebrate #RareDiseaseDay2025, I spoke to @Labiotech.EU about long-read sequencing’s vital role in progressing rare disease research and improving the diagnostic pathway. 🧬 Read the full article here.👉 https://t.co/qbTPyq9w2O
#Genomics
labiotech.eu
As we observe Rare Disease Day today, let us take a look at seven drugs poised to be approved to address rare diseases in 2025.
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Today in @FT, I discuss the importance of ramping up biosurvelliance of animal microbiomes to reduce the risk of zoonotic pathogens spilling over into human populations. Read my response to @Michaelpeeljourno’s article here. 👉 https://t.co/tCvTok3Lzt 🔗 #Genomics #PacBio
ft.com
From Neil Ward, Vice-President and General Manager Emea, PacBio, London N7, UK
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Our new Nature Genetics paper on human segmental duplications (SDs) provides a pangenome perspective of SDs, new potential protein-coding genes, and greater complexity in human variation with implications for disease and evolution. https://t.co/CYCI8xQEiH
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In @Manchempharma, I discuss the future of #pharmacogenomics. This year will see large-scale PGx research integrate health records, drug response and genetic data at the population level to drive advances in #PrecisionMedicine.🧬 Read more here. 👉 https://t.co/0yVWEsRUAN
manufacturingchemist.com
Neil Ward, VP EMEA of PacBio, takes a look at the near-term future of pharmacogenes
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In @DDDMag, I discuss how advances in long-read sequencing, increasing biobank participation, and pharmacogenomics will transform the diagnosis and treatment of diseases in 2025. 🧬 Read the full Q&A, here. 👉 https://t.co/LQYoVyVCEw
#Biobanks #PrecisionMedicine
drugdiscoverytrends.com
National biobank initiatives are set to drive precision medicine through genomic data analysis by 2025, according to Neil Ward, a PacBio VP.
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In @Laboratorynews, I discuss the role of biobanks in revolutionising precision medicine. 🧬 I explain how the @ESTbiobank is using genomic insights to better understand the factors influencing public health and disease. Read more, here 👉 https://t.co/Ct24EkYsLI #Biobanks
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In @InsideEcology, I discuss the role of #GenomicSequencing in tackling #biodiversity loss. 🧬 @Darwintreelife is one example of how the UK is harnessing genomic insights to understand species’ health and inform #conservation efforts. 🌍 Read more, here. 👉 https://t.co/xGkTCkWt28
insideecology.com
Neil Ward, VP PacBio EMEA Loss of biodiversity in the UK is currently outpacing conservation efforts to tackle it, with almost 1 in 6 species now at risk of becoming extinct. In fact, since 1970, the...
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NEW: Learn how the new SPRQ chemistry for #Revio is improving long-read #sequencing performance and affordability like never before: https://t.co/mgNFywDIcR
#PacBio #ASHG24
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