Join us for our next #webinar “Long-read sequencing, the next era of genomics” with special guest speaker Thea Ziegler, Sequencing Application Sales Specialist at PacBio and Novogene Europe Deputy Director of Product Marketing, Shi-qi An PacBio highly accurate long-read sequencing provides one of the most comprehensive views of #genomes, #transcriptomes, and #epigenomes. In this webinar we will present new trends in the genomics field as well as an overview of major applications. The new Kinnex applications increase throughput for full-length RNA, single-cell RNA, and 16S sequencing on PacBio long-read sequencing systems to enable large-scale studies at extraordinary resolution. Webinar date: 10am BST/11am CEST Tuesday 23rd July 2024. Register here: https://bit.ly/3VUk2Ow Key takeaways: · Understand the principle and advantages of highly accurate long-read sequencing to explore the full spectrum of genetic variation · Gain an overview of the most important applications, including whole genome sequencing, targeted sequencing, RNA sequencing and microbial genomics · Understand how PacBio long-read sequencing of extended 16S amplicons enables identification of metagenome community members at higher taxonomic resolution than common methods · Learn how Kinnex full-length RNA and single-cell RNA sequencing enables scientists to capture full-length isoforms, elucidating isoform diversity in development and disease Webinar date: 10am BST/11am CEST Tuesday 23rd July 2024. Register here: https://bit.ly/3VUk2Ow #Sequencing #Revio #NGS
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Decoding Life's Blueprint: Navigating the Dynamics of the DNA Sequencing Market Request Free Sample Report:https://shorturl.at/gETV6 The DNA Sequencing Market stands at the forefront of scientific innovation, unlocking the secrets encoded in the building blocks of life. This transformative technology has revolutionized genomics, enabling researchers and healthcare professionals to unravel the complexities of genetic information with unprecedented speed and precision. From unraveling the mysteries of rare diseases to tailoring personalized medicine, DNA sequencing has far-reaching implications across diverse fields. The market is witnessing a rapid evolution marked by continuous advancements in sequencing technologies, reduced costs, and increased accessibility. As the demand for high-throughput, accurate, and cost-effective sequencing solutions grows, the DNA Sequencing Market continues to be a driving force in propelling genomics research and clinical applications forward. #Genomics #DNASequencing #PrecisionMedicine #GenomicResearch #BiotechInnovation
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🔬 Exciting advancements in genomics are transforming personalized medicine! Next-Generation Sequencing (#NGS) technology, with its high-throughput capabilities, enables rapid and cost-effective DNA/RNA sequencing. Discover more with this #Personalized_Medicine_Bioinformatics series by Zena Jandali The book link https://lnkd.in/dU3Dr4qx
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With The WOLF Cell Sorter, researchers can easily isolate viable cell samples for genomics workflows before sequencing: 1. Save time (and money!) by saying goodbye to unwanted dead/dying cells and intrusive debris 2. Gentle cell sorting enables you to enhance sample quality, setting the stage for successful genomic sequencing. Webinar: October 18 @ 1pm BST/WAT | 2pm CEST| 3pm EAT Title: Enhancing Genomics Sequencing Data with Gentle Cell Sorting
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The density of information per cell researchers are getting with ResolveOME is astounding. #singlecell #multiomics #transcriptomics #genomics
ResolveOME™ provides a more complete picture of the drivers and consequences of clonal heterogeneity within cell populations than ever before. ResolveOME whole genome and transcriptome amplification system: · Enables whole genome and transcriptome sequencing from a single cell · Provides industry-leading genomic coverage and resolution · Facilitates superior transcriptome capture and coverage · Fits into established laboratory protocols · Scales to experiment size · Features bioinformatics analysis See how ResolveOME can elevate your next research project with our unique single-cell multiomic analysis technology. Contact us here: https://lnkd.in/eMVbeGd2 #genomics #singlecell #multiomics #research
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Senior Field Applications Scientist at illumina. Improve human health by unlocking the African genome
🌟 Experience the Power of Genomics with Illumina! 🌟 If you're as fascinated by genomics as I am, you absolutely need to check out Illumina’s latest omics solutions. They’re transforming the field with some seriously cool tech for Whole Genome Sequencing (WGS), Whole Exome Sequencing (WES), targeted Amplicon panels, and RNA sequencing with seamless automation. Illumina’s solutions make it practical and easy to conduct comprehensive genomic research and clinical diagnostics. 🔬 And it gets even better! Illumina's data analysis solutions, such as the DRAGEN platform and Emedgene for germline interpretation, use artificial intelligence to make data analysis a breeze. It’s like having a genomic superhero team at your fingertips. Whether you're diving into clinical diagnostics, pioneering new research, or just love cutting-edge science, Illumina’s tools can help you achieve incredible breakthroughs faster and more cost-effectively. I strongly recommend you explore how these technologies can elevate your work and spark new discoveries. Check Illumina Genome Solutions (https://lnkd.in/d8bN4GeF) #Genomics #Innovation #Illumina #WGS #WES #TargetedPanels #RNASequencing #Automation #DRAGEN #AI #GenomicResearch #PersonalizedMedicine
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Please join us for this week's Dovetail Genomics Ask the Experts webinar: Demystifying Hi-C Data Normalization November 15th at 8:00 am PST Presented by Dr. Myriam El Khawand and Dr. Jonathon Torchia Genomic research has come a long way since the draft of the human genome was first published over two decades ago, driven by continuous advancements in next-generation sequencing (NGS) technologies. One of the most transformative methods to emerge from these developments is Hi-C, a library preparation technique that provides unique insights into the three-dimensional organization of the genome. However, analyzing Hi-C data presents its own set of challenges, particularly regarding data normalization. In this webinar, we'll delve into the intricacies of Hi-C data normalization, providing you with an understanding of its importance and the various tools and methods available for this critical step in the analysis pipeline. Register here to attend or receive the recording: https://ow.ly/IUxT50Q7A7T
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Data Operations Lead (Senior Manager) for Imaging OMICS platform at Global Innovation & Technology Centre (GITC), AstraZeneca
good opportunity
Great opportunity to learn about single cell genomics!
2nd Hands-on workshop on single cell genomics using 10x Genomics and its data analysis
indiabioscience.org
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Head of Life Science Division @ Kinetica | North America, Europe & APAC Recruitment Solutions | 12,000+ Followers
BioSkryb Genomics has announced the launch of its groundbreaking ResolveDNA Whole Genome and ResolveOME Whole Genome and Transcriptome Single-Cell Core Kits, marking a significant leap forward in single-cell multiomics research. These cutting-edge kits harness the power of primary template-directed amplification, delivering not only efficient workflows but also industry-leading insights into single-cell DNA. With streamlined processes taking less than eight hours, researchers can now delve into the intricate details of clonal architectures and gain invaluable insights into disease pathogenesis using longitudinal samples. What's more, the ResolveOME kit goes beyond conventional approaches by seamlessly integrating DNA and RNA from every cell, eliminating the need for cumbersome sample splitting. This integration not only simplifies the workflow but also ensures comprehensive multiomic analysis, providing researchers with a holistic view of cellular processes. Powered by BioSkryb's innovative BaseJumper platform, comprehensive data analysis and visualization are now at researchers' fingertips. Additionally, ResolveServices™ offers tailored solutions such as the ResolveXOME exome enrichment solution and custom DNA panels, enabling researchers to customize their genomic analyses to suit their specific research objectives. With BioSkryb's cutting-edge technologies and customizable solutions, researchers can now unlock the full potential of single-cell multiomics with unprecedented ease and precision. #genomics #singlecell #multiomics #dnaanalysis #research #biotech
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Strand Life Sciences's Genomic Health Insights Program analyzes 20,000+ genes with Next Generation Sequencing and proprietary bioinformatics tools. 🧬🧪 #StrandGenomicWellness #GeneticTesting #InformedDecisions #DNA #ComprehensiveGeneticTesting #Wellbeing
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