Nostos Genomics’ Post

We’re thrilled to announce that Anderson Diagnostics will be part of the 34th KSOGA Conference 2024 in Hassan! Visit our stall between 8th and 10th November, where we’ll showcase the latest genetic diagnostics. From groundbreaking technologies in preimplantation genetic testing to the future of personalized healthcare, our experts are here to guide you through the potential of genetic testing. Discover how we are helping shape the future of healthcare through innovative diagnostics. We can’t wait to connect with you! #AndersonDiagnostics #KSOGA2024 #GeneticHealthcare #PersonalizedMedicine #GeneticTesting #MedicalInnovation #WomensHealth #Genomics #HealthcareTechnology #MedicalConference #InnovativeDiagnostics

Are you attending Association for Clinical Genomic Science (ACGS) today (10 June)? If so, make sure to catch a really insightful talk - A Spectrum of Possibilities: Our Experience by Dr David Brettle of Royal Surrey County Hospital at 3.10 p.m. #ACGS #genomics #clinicalgenomics

The COL1A1 and COL1A2 genes, responsible for encoding type I collagen, play a vital role in maintaining connective tissue strength. Variants in these genes are the primary cause of Osteogenesis Imperfecta (OI), a condition characterized by fragile bones, frequent fractures, and other connective tissue-related complications. Osteogenesis Imperfecta is a stark reminder of the importance of early and accurate genetic diagnoses. In a blog we shared earlier, we highlighted our colleague’s remarkable journey in her fight to secure the correct diagnosis for OI. Her story reflects the struggles many face with rare diseases and the critical role genetic insights play in providing answers. At Genomenon, we are proud to support the rare disease community through curated genetic data, helping clinicians and researchers uncover the root causes of complex conditions like OI. By connecting patients’ stories to the science behind the diagnosis, we strive to bring hope and clarity to those navigating the diagnostic journey. 🔗 Revisit Jessica’s story here: https://lnkd.in/gMHkTy6v #OsteogenesisImperfecta #COL1A1 #COL1A2 #GenomicIntelligence #Genomics #Genetics #MastermindGIP

ADLM 2024 Highlights: Gain insight into the mission and values guiding LGC Biosearch Technologies and LGC Clinical Diagnostics. Explore their extensive range of products and services, the strategic collaboration between these two branches, and their commitment to advancing the future of clinical diagnostics and genomics. Watch more videos on SelectScience: https://lnkd.in/eDAqpYee #clinicaldiagnostics #clinicalscience #genomics #ADLM2024

Three ways that SynGAP Research Fund has made #SYNGAP1 research easier: 1) more disease models: mice and iPSC lines, 2) biomarker studies, 3) genetic variant visualization rich with data. Come to the 2024 SRF Conference in LA! Register at Syngap.Fund/LA! #SyngapConf #SyngapConf24 #CureSYNGAP1

Are you attending Association for Clinical Genomic Science (ACGS) on 10 June2024? If so, pop by to have a chat with some of our team, and make sure to catch a really insightful talk - A Spectrum of Possibilities: Our Experience by Dr David Brettle of Royal Surrey County Hospital at 3.10 p.m. that day. #ACGS #genomics #clinicalgenomics

Just how many samples do you need to see causal links and downstream effects of genetic variants? Use our coefficient of variation (CV) calculator to see how few samples your study needs – and still have the industry's highest reproducibility: https://bit.ly/3QFiBRh  Curious to know more? Read published research on the benefits of a proteogenomic approach using the SomaScan® Assay: https://bit.ly/3QFiBRh #biomarkers #drugdiscovery #drugdevelopment #proteomics #genomics

Could your genetics hold the key to how severely COVID-19 impacts you? 🧬 Explore how PAI-1 polymorphisms may play a crucial role in COVID-19 severity and uncover the potential for personalized treatments based on genetic insights here: https://bit.ly/3UodYh7 Check out this fascinating article for more details and share your thoughts in the comments—how do you think genetics shapes disease outcomes? #COVID19Research #Genomics #PersonalizedMedicine

While attending ADLM 2024, Ken Yoon and Bharathi Anekella spoke to SelectScience about the mission and values driving LGC Biosearch Technologies and LGC Clinical Diagnostics. Learn about our wide range of products and services, the collaborative synergy between the two branches, and the vision for advancing the future of clinical diagnostics and genomics: https://hubs.li/Q02Pq18S0 #ADLM2024 #clinicaldiagnostics #genomics

🌟 New Research Alert! 🌟 Explore Mitophagy-Related Genes in Sepsis! Our latest article, “Identification of Mitophagy-Related Genes in Sepsis,” uncovers critical insights into how mitochondrial autophagy can influence the onset and progression of sepsis. 🔍 Key Findings: Identified four key genes associated with mitophagy: TOMM20, TOMM22, TOMM40, and MFN1. Provides a foundation for future biological studies aimed at sepsis treatment. Published in Volume 19, Issue 8, 2024, this open access article is now available! 👉 Read it here: https://bit.ly/4dWpjvL Join us in advancing the understanding of sepsis and its treatments! #Sepsis #Mitophagy #MitochondrialHealth #OpenAccess #MedicalResearch #Biology #Inflammation #Healthcare #Genomics #ProteinInteraction