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
Source BioScience的动态
最相关的动态
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I am looking forward to presenting in this seminar series. I will present our recent work on the #epigenetic regulation of #transposons in stem cells during development and #placental disorders. #preeclampsia
Our first session of our new Virtual Seminar Series, 'The 3D Regulatory Genome' is fast approaching! Join us for an exciting seminar with guest speaker Dr Pradeepa Madapura from the Blizard Institute. ?? November 7, 2024 ? 16:00 GMT ?? Virtual (Zoom link sent upon registration) Join our 3D Genomics Professional Network to register: https://lnkd.in/eitEtkfj #VirtualSeminar #Genomics #3DGenomeOrganisation #EnhancerRoles
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If you are at LRUA today, come grab a PacBio cupcake ?? ?? and make your way over to our feature worksop 'Now to Next - the future of genome sequencing is closer than you think' at 10:45 AM. Hear Michael Eberle, Carola Greve, and Christian Betz present how HiFi sequencing can accelerate your work. #LRUA24 #Genomics #HiFiSequencing
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“Step into the lab with me as I dive into Pyrosequencing! From DNA isolation and PCR amplification to the final sequencing reactions—each phase demands accuracy and focus. Here’s a glimpse of how we decode genetic sequences, one nucleotide at a time. #PhDLife #Pyrosequencing #Genomics #MolecularBiology”
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Are you attending #PAG2025? Curio Genomics is collaborating with Revvity to provide a low-pass sequencing and imputation solution. Get 10x more data than microarrays at a fraction of the cost of high-depth WGS. Stop by CURIO Genomics booth #331, to learn more about it. https://ms.spr.ly/6043otG0f #PlantGenome #AnimalGenome #Genomics #PAGConference For research use only. Not for use in diagnostic procedures.
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Explore the future of genomics with our on-demand webinar: "Maximizing Genomic Insights: An In-Depth Look at Long-Read Sequencing." Discover how long-read sequencing empowers research with comprehensive insights into complex regions and structural variants. Watch now: https://ow.ly/WsZQ50UeVFb #LongReadSequencing #Genomics #StructuralVariants #SequencingTechnology #GenomicsResearch
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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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On #EvolutionDay, we celebrate not just the theory of evolution, but the evolution of science itself! At Novogene, our cutting-edge genomic sequencing services help researchers unlock the secrets of life’s evolution, from plants to animals, and everything in between. Ready to evolve your research? Learn more about our services: https://ow.ly/ZW4q50TWb2a #Genomics #Research #Innovation
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Attending #PAG2025? Visit CURIO Genomics at booth #331 to learn about the new low-pass sequencing and imputation solution with Revvity enabling researchers to get 10x more data than microarrays at a fraction of the cost of high-depth WGS. https://ms.spr.ly/6042otGAi #PlantGenome #AnimalGenome #Genomics #PAGConference For research use only. Not for use in diagnostic procedures.
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Learn why Anna Lindstrand of Karolinska Institutet believes long-read technology is set to revolutionize clinical genomics and why it's the future we should embrace. While many labs are content with exome sequencing, Anna believes that long-read whole genomes will become the preferred choice. #WelcomeToTomorrow #PacBio #Genomics
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Join Kendall Lee from Veil Genomics - a HudsonAlpha company - as she explores the transformative power of long-read low-pass sequencing for variant detection. Learn how our LongPlex? Long Fragment Multiplexing Kit maximizes long read sequencing scalability and improves variant detection accuracy. #seqWell #LongPlex #Genomics #LowPass #LongRead https://hubs.ly/Q032Qqxx0
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