?? Join our team at booth #20 at the 2024 Human Genome Meeting (#HGM) in Rome with our partner Euroclone SpA and discover how we can elevate your NGS and spatial research to the next level. ?? We also have some exciting giveaways up for grabs! ?? On April 10th at 13:00 in the Parallel Hall, we will be hosting a Corporate Symposium where Dr. Antonio Grimaldi from the Telethon Institute of Genetics and Medicine will speak on “Benchmarking of short reads sequencing in clinical genomics.” He will discuss the importance of applying genomics in clinical settings, contributing to medical solutions better suited to the specific genetic needs of the population in Italy and beyond. Come and connect with our Europe and Africa team in person! Bernard Okere, André Sousa, Lindsay Tseng, Bret Wurdeman, Javier Batista Perez #MGI #EUROCLONE #HGM2024 #DNBSEQ #NGS #omicsforall #Genomics #Sequencing?
MGI的动态
最相关的动态
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?? Exploring Ultraconserved Elements (UCEs) for Bivalve Phylogenetics ???? Discover how Next Generation Sequencing revolutionized DNA analysis, making phylogenomics more accessible than ever. This study by Harvard University delves into UCEs to resolve complex family relationships across Bivalvia, using innovative probe sets and computational tools like CIPRES for robust phylogenetic inference. #Phylogenomics #NextGenSequencing #UCEs #BivalvePhylogenetics #EvolutionaryBiology #Genomics #CIPRES #ResearchHighlights https://buff.ly/3TbdOJk
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We’re thrilled to have Dr Leslie Biesecker from the National Institutes of Health (NIH) present at our next DNA dialogue seminar on Thursday 30 May at 9am (AEST). Dr Biesecker will talk about evolving guidelines for variant classification. The variant classification categories used widely in today’s clinical genetic and genomic testing derived from recommendations of the American College of Medical Genetics and Genomics. The five categories are: pathogenic, likely pathogenic, uncertain significance, likely benign, and benign. The ACMG is drafting what will be the fourth iteration of guidelines for the general variant classification framework. These new guidelines will incorporate a number of recent advances including a mathematical framework, incorporating objective, quantitative assessments of evidence, and the subdividing of the VUS category. Learn more & register here: https://lnkd.in/gEeF4mbp National Human Genome Research Institute (NHGRI) #AustralianGenomics #DNAdialogue #SeminarSeries #genomics #research #variantclassification?
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Reproducibility is a foundational challenge in scientific research, especially with the complex datasets generated by next-generation sequencing (NGS) ?? ATCC is leading the way by providing authenticated, high-quality reference materials that enhance the reliability of NGS data across applications in genomics, metagenomics, and microbiome studies. Read this blog to learn about the importance of authenticated reference materials and how they support greater consistency and reproducibility in sequencing data: https://okt.to/sYSxQP #Reproducibility #NextGenSequencing #Genomics
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If you missed Julie Eggington, MS, PhD's talk with Stanford University's METRICS program titled "?????????????? ???????????????? ???????????????? ???????????????? ?????? ????????????????: ?? ???????????? ???? ?????? ???????????????? ???????? ???????? ???????????????????????? ???????? ???????????? ?????????????????????? ?????? ???????????? ???????????????? ?????? ???????? ?????????????? “?????????????????? ????????????????” ???? ?????? ??????" here it is on YouTube: https://lnkd.in/gupCkqtR Dr. Eggington ran out of time to share what stakeholders can do about the issues presented, so if you would like to learn more, please reach out to us directly. #ELEVATEGENETICS #PrecisionMedicine #PrecisionOncology #ClinicalGenetics #Genomics #RareDisease #NGS #NextGenerationSequencing #GCChat #FDA #CLIA #LaboratoryDevelopedTests #LDTs #MedicalMalpractice
Reality Checking Clinical Genetics and Genomics - Julie Eggington
https://www.youtube.com/
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GenieUs Genomics, in collaboration with Duke University and Temple University, just announced a pioneering precision health approach for ALS. The "ROAR-DiGAP" study utilizes the DiGAP? platform for comprehensive genomic profiling, aiming to uncover genetic variants and stratify ALS subtypes. We are excited to share that PacBio technology is powering this groundbreaking study with the Revio system and our exceptional HiFi long-read sequencing. Learn more about the study here: https://bit.ly/4bfcHyA #ALS #PrecisionMedicine #Genomics #PacBio
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GenieUs Genomics, in collaboration with Duke University and Temple University, just announced a pioneering precision health approach for ALS. The "ROAR-DiGAP" study utilizes the DiGAP? platform for comprehensive genomic profiling, aiming to uncover genetic variants and stratify ALS subtypes. We are excited to share that PacBio technology is powering this groundbreaking study with the Revio system and our exceptional HiFi long-read sequencing. Learn more about the study here: https://bit.ly/4bfcHyA #ALS #PrecisionMedicine #Genomics #PacBio
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Sharing an exciting (and free!) #omics talk sponsored by 10x Genomics, "The State of Omics 2024", occuring Wednesday April 17 that might interest some folks: https://lnkd.in/e9fyQFQf Learn how advances in #NGS and its applications are providing critical insights into the biology of health and disease. #proteomics #spatialbiology #singlecellbiology #spatialomics #genomics
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We are proud to partner with Stilla Technologies. Together, leading the way in the UK and Ireland as the first provider to bring the NIO Digital PCR System to researchers. At Source Genomics, we’re committed to empowering researchers with the tools they need to make life-changing discoveries. Read the press release here ?? https://lnkd.in/evPu_h_Z #MolecularDiagnostics #GeneTherapy #StillaTechnologies #dPCR #Genomics #TheSequencingPeople
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?? Future of Omics Interview Highlight ?? Exciting insights from our recent interview at Future of Omics Conference with André G. Uitterlinden, professor at Erasmus Medical Center! He shared his experiences coordinating the Genome of Europe, 1 Million Genomes initiative (1+MG), a groundbreaking large population genomics project. This initiative aims at sequencing 100,000 whole genomes and capturing the genetic diversity across the European continent.? Check it out and see what his opinion is. #FutureofOmics #seqALL #1MillionGenomesinitiative #1MG #Europe #PopulationGenomics
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???Explore RNA-Seq!??? Join our tutorial on bulk & single-cell RNA sequencing and take your genomics research to the next level! Perfect for beginners and experienced researchers alike. Don't miss this opportunity to dive into cutting-edge techniques! #RNASeq #Genomics #ResearchTools #MultiOmics
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Regional Sales Manager EMEA South at Cytiva | Genomics Medicine | Healthcare Passionated
11 个月Champions league level ??