There is no doubt that the field of #genomics is advancing rapidly, with new discoveries appearing seemingly every day that are likely to have a profound impact on how #healthcare is delivered in the future. Although #research is going well, we have yet to see the necessary shifts in #clinicalpractice that will translate these scientific advances into better #patientcare at the #bedside. #genetics #precisionmedicine #translationalmedicine #translationalresearch
Dr. Nael Ismail’s Post
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Senior Clinical Research Nurse & Team Lead, Guy's and St Thomas' NHS Foundation Trust & Co-founder of Nurture Nursing Ltd
Such a privilege to be attending the #understandinggenomics in the #NHS conference today. A morning of fantastic speakers and interesting debates on not only the practical application of #genomics in #clinicalpractice but also wider social issues that this field of study raises for our society. I look forward to the rest of the day! #innovationinhealthcare #innovationinmedicine #genetics #nurseleaders #clinicalresearch #clinicalresearchnurse
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📢 Current Promotion: Discover the power of our GSA service! Unlock insights into genetic variation, disease, and pharmacogenomics with our Infinium Global Screening Array. Customisable booster options, multi-ethnic genome-wide coverage, and high throughput processing make it perfect for your application. Learn more today! 💻 https://lnkd.in/eCyf3qyu #agrf #genomics #genetics #research #populationgenomics #globalscreeningarray
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We wanted to remind you that our special Global Screening Array (GSA) 10% discount offer is coming to an end on Monday 17 June 2024. Our GSA service offers flexibility and affordability for population genetics, pharmacogenetics, disease studies and more, empowering researchers like you with expertly curated global content, providing insights that drive ground-breaking discoveries. Here's why our Illumina Infinium GSA stands out: 🔹 Flexible Solutions: Tailored to meet the diverse needs of genetic research, our GSA service offers flexibility in study design, sample types, and data analysis. 🔹 Affordable Innovation: We understand the importance of cost-effective solutions without compromising on quality. Our GSA service provides affordability without sacrificing accuracy or depth of data. 🔹 Expertly Curated Content: With curated content from around the globe, including diverse populations, our array ensures comprehensive coverage for a wide range of research applications. 🔹 Customisable booster content available. Whether you're exploring population genetics, investigating disease pathways, or delving into pharmacogenetics, our GSA service is your gateway to transformative insights. Are you ready to take your genetic research to the next level? Reach out to our team today to learn more about how our service can accelerate your research goals. 📧 [email protected] Promo Code: ARRAYS050524 #PopulationGenomics #GenomicsResearch #GeneticAnalysis #ResearchTools #ScienceDiscount #DiscoveriesAwait
📢 Current Promotion: Discover the power of our GSA service! Unlock insights into genetic variation, disease, and pharmacogenomics with our Infinium Global Screening Array. Customisable booster options, multi-ethnic genome-wide coverage, and high throughput processing make it perfect for your application. Learn more today! 💻 https://lnkd.in/eCyf3qyu #agrf #genomics #genetics #research #populationgenomics #globalscreeningarray
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Variants of uncertain significance (VUS) for aHUS https://lnkd.in/echui7Kg Our article highlights a podcast by NHS England’s Helen Brittain, Clinical Lead for Rare Disease Diagnostics at Genomics England . #complement #aHUS #atypicalHUS #NHS #genetics #genome
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[BLOG] LINE-1 Elements Walk the LINE. Transposable elements served a purpose in human evolution, but these days LINE elements are of interest for their role in disease & #aging. Check out the blog: 🎵 https://bit.ly/48v3qB6 #genomics #genetics #epigenetics #cancerresearch #chromatin
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NERDGENE. A new wave in GENOMIC TESTING is here. Here to help you help make informed decisions about you and your family's health through precision medicine. To know more about us, tap the link in bio. 🧬 #NerdGene . . . #genomics #genetics #genomictesting #genetictesting #dna #genome #health
NERDGENE. A new wave in GENOMIC TESTING is here.
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Working on rare diseases? Our DECIPHER database gives you access to publicly available patient data allowing simple phenotypic and genotypic data comparisons. The latest DECIPHER database release covers a host of new features including: ➡️Integration of AlphaMissense scores from Google DeepMind to help you estimate how likely a nucleotide missense variant is to be pathogenic ➡️ Gene pages now link to the Open Targets Platform, facilitating the identification and prioritisation of potential therapeutic targets ➡️New Genome Aggregation Database (gnomAD v4.1) copy nucleotide variation (CNV) genome browser track displaying rare coding autosomal CNVs from exome sequencing of over 450,00 individuals Find out more here 👇 https://lnkd.in/eDFnQbCT #genetics #genomics #bioinformatics #raredisease
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In the ever-evolving field of #genetics, understanding the relationship between genes and diseases is crucial for improving patient care. Join Jennifer Herrera-Mullar to explore the importance of gene-validity scoring, the evolution of GDV frameworks and the future of #GDV curation. https://hubs.ly/Q02DH-K80
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Here are a few things that genomic medicine can do. #genome #genomics #genomicmedicine #genomeediting #genes #genetics #geneticmodification #genomicsforall #mibiometherapeutics
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