🎉 Congratulations, Joris Veltman! 🎉 Joris will receive $3,000 in GenFind V3 reagents for work on long-read whole genome sequencing using the PromethION. 🧬 Through our SPRI Grant Program, we provide $3,000 worth of DNA/RNA reagents to researchers who are exploring new avenues in genomics and pushing the boundaries of scientific discovery. Interested? Learn more and apply here: https://becls.co/4csPaLO #Genomics #Reagents #GrantProgram
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📣 NEW WEBINAR SERIES! Decoding complexity: Tackling real-world challenges in variant analysis. Tune in for the first episode of our webinar series named "Overcoming noise in precision variant analysis ". In this episode, Dr. Xiaobin Xing, Director of Bioinformatics at SOPHiA GENETICS explains how signal amplification and noise suppression can increase the analytical performance of NGS applications. 💡In this webinar hosted by Dr. Iole Pezzuto, Dr. Xing is sharing real-world examples of the strategies employed by SOPHiA DDM™️ to accurately detect challenging variants, important for specific applications from liquid biopsy to homologous recombination deficiency (HRD), and pharmacogenomics to RNA sequencing for fusion detection. 🎥 Watch the webinar: https://loom.ly/OJ2w5Sk #webinar #genetictesting #NGStesting #genomics #biotechnology #DNAsequencing #liquidbiopsy #HRD #datadrivenmedicine #AIinHealthcare #futureofhealthcare
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See what you’ve been missing. ResolveDNA® provides industry-leading uniformity and accuracy, giving scientists the resolution for groundbreaking discoveries. The ResolveDNA whole genome amplification system: • Enables whole genome sequencing from a single cell • Provides industry-leading genomic coverage • Results in unprecedented single nucleotide variant (SNV) calling resolution • Fits into established laboratory protocols • Scales to experiment size • Includes bioinformatics analysis How can BioSkryb help unlock your discovery potential? Get in touch to find out: https://lnkd.in/eSUzQtNM #genomics #singlecell #multiomics #research
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SOLUTION: Sequencing Technologies for DNA 5mC/5hmC Modifications About the Solution With the development of next-generation sequencing technology (NGS) and third-generation sequencing (TGS), modifications including but not limited to 5mC and 5hmC can be analyzed genome-wide. These technologies are so-called "DNA methylation sequencing" and allow access to genetic information beyond traditional genomics research. This infographic will present you with the basic information regarding DNA modifications, 5mC and 5hmC, as well as the related sequencing technologies that can be used as tools. https://lnkd.in/ecPkCygR
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NGS| Next-Gen Sequencing| NGS Insights for Beginners #NGS #genomics #bioinformatics #bioIT #biotech #biopharma #omics #biology Welcome to Molelixir Informatics Channel! In this video, we delve into the fascinating world of Next-Generation Sequencing (NGS). Discover the revolutionary technology behind NGS and learn how it is reshaping genomics research. Whether you're a student, researcher, or just curious about the future of genetic exploration, this video is your gateway to understanding NGS techniques and applications. Dr Jyoti Bala
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Nanopore sequencing is a cutting-edge genomic technology that allows for the direct, real-time analysis of DNA or RNA at the level of individual molecules. The process involves passing the genetic material through a nanoscale pore, and the changes in electrical current as the molecules pass through are used to identify and sequence the nucleotides-building blocks of DNA or RNA. Submissions are open for the upcoming issue. You may submit case reports, case studies, and research or review papers. Submit to: [email protected] Follow our page: https://lnkd.in/dd-AwMD8 Visit us: https://lnkd.in/dhyieEcT (Source: internet) #NanoporeSequencing #Genomics #Nanotechnology #DNASequencing #ScientificInnovation
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In this webinar, see for yourself the value of miniaturizing NGS library preparation using mosquito®, our innovative nanoliter pipettor. With over 40 examples of miniaturized protocols, mosquito is proven to help you deliver the high throughput, cost-effective sequencing that modern genomics research requires. Learn how mosquito can pay for itself in just tens of DNA or RNA sample plates, and open the way for cost-effective NGS with accessible, quality liquid handling automation. Watch Now: https://bit.ly/43UfT0I #LiquidHandling #Webinar
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Next-Generation Sequencing (NGS) has revolutionized both our understanding and utility of genomics, marked by a surge in direct-to-consumer genomics and transformative therapeutic advancements. As applications and method developments increase, more challenges are also revealed in the NGS landscape. AUGenomics CEO Hannah Dose talks logistical challenges in NGS as a sequencing service provider, and the strategic solutions that save time and resources. Watch the full video: https://lnkd.in/gUhFX6n6 #genomicsequencing #exomesequencing #bioinformatics
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🚀 Excited to share that I’ve just completed an insightful webinar on reagents for the Advanced Genomic Course! 🧬 This learning journey deepened my understanding of critical milestones in genomics, from the Human Genome Project's groundbreaking achievements to the rise of CRISPR technology. These advancements are revolutionizing personalized medicine and genetic research. Currently, I am thrilled to contribute to this dynamic field by applying these advanced techniques to enhance genomic research and innovation. #Genomics #AdvancedGenomics #CRISPR #PersonalizedMedicine #ContinuousLearning #WebinarSuccess #Biotech
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Ready to take your multiomics analysis to the single-cell level? Schedule a meeting with BioSkryb at #AGBT24 or stop by Antigua 1 to learn how we provide the most comprehensive view of the genome, transcriptome, and targeted proteins at single-cell resolution. Learn how the next generation of single-cell technology: - Enables whole genome and transcriptome sequencing from a single cell - Provides industry-leading genomic coverage and resolution - Generates superior transcriptome capture and coverage - Integrates DNA, RNA, and targeted protein analysis from individual cells Schedule a meeting or stop by Antigua 1 and talk with BioSkryb’s experts to discover the future of single-cell analysis. https://lnkd.in/eQ28Y3f6 AGBT - Advances in Genome Biology and Technology #genomics #cancerresearch
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The goal of #DNADay is to help students, teachers, and the public learn more about #genetics and #genomics. As part of this, it's incredibly important to put #DNA in context. Our genomes provide blueprints for the parts that make up our bodies, but we cannot predict biological outcomes from genetic information alone. Proteins, RNA, metabolites, and interactions with the environment profoundly increase the complexity of biological systems. Studies of all these levels of #biology must complement genomics for us to truly understand how life works.
Happy #DNADay! Decades of progress in #genomics research have built a foundation for our understanding of #biology and its incredible complexity. Now we must dive deeper to learn about the interactions between genes, RNA, and proteins through #proteomics, the study of all proteins in a biological system. Read more on our blog about how proteomics complements genomics and how combining both approaches can drive new innovation in biomedicine and fundamental research: https://ow.ly/9rLe50RoiRX #DNADay24 #NationalDNADay #UnleashTheProteome #ProteomicsRevolution #MassSpectrometry #TeamMassSpec #Biotech
Genomics vs. proteomics: Two complementary perspectives on life
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