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🔬✨ Don't Miss Our Exclusive Webinar Tomorrow! Join us tomorrow at 1:30 PM (Swiss time) for an in-depth webinar presented by our Ionic specialist, Michael Colombo. Discover how the Ionic system by Bionano is revolutionizing genomic research with isotachophoresis. Learn how to: - Achieve higher yields in DNA and RNA isolation - Implement simpler workflows to save valuable time - Reduce fragmentation for more reliable results This technology is a game-changer for anyone working with FFPE samples. Whether you're in biotech, life sciences, or genomic research, this webinar will provide invaluable insights to elevate your work. 🚀 Register now to secure your spot and stay ahead in your research: [https://lnkd.in/gfbSKhDu) ⏰ Hurry, registration closes soon! #GenomicResearch #DNAIsolation #RNAIsolation #Biotech #LifeSciences #ResearchInnovation #Webinar #FFPE #LabTech

🔬 Benchmarking Commercial Single-Cell Transcriptomics: A New Comparative Analysis 📊🧬 Published a recent paper by Marco De Simone et al. on bioRxiv, "Comparative Analysis of Commercial Single-Cell RNA Sequencing Technologies." The study evaluates 10 commercially available scRNA-seq approaches across four technology groups using PBMCs from a single donor. 🛠️ Technology Groups 🛠️ 🟣 Emulsion-based kits: 10x Genomics, Fluent Biosciences 🟢 Microwell-based kits: Becton Dickinson, Honeycomb Technologies, Singerlon Technologies 🟠 Combinatorial-indexing kits: Parse Biosciences, Scale Biosciences 🔵 Matrigel-based kit: Scipio Biosciences ✨ Key Findings ✨ 📈 10x FRP excels in gene and UMI detection but is limited to human and mouse genomes and incompatible with genotype-based demultiplexing tools. 🔍 The study underscores the importance of choosing scRNA-seq kits based on specific experimental needs, considering cell type, cost, and throughput. 📚 bioRxiv paper: https://lnkd.in/dYqX6ea9 👨💻 GitHub: https://lnkd.in/d_qHMhdu 📢 Join the Conversation 📢 Share your ideas, methods, and tools in the comments! 👇 💬 #SingleCellRNAseq #Bioinformatics #PharmaInnovation #Biotechnology #Genomics #Research #scRNAseq #BioRxiv

Stuck with Pathway Analysis? Tools not working? Or it’s just you? Let’s break & understand, Save the date & Join us for a free online coffee break with Alexander Kel from geneXplain & get it sorted. Yes, you read it right, it’s free. . . . #bioinformatics #genexplain #transfac #Pathway #biotechnology #Industry #Seminars #biology #Free #

🌟 Unlock the Future of Genomics with Macrogen CES 🌟 At Macrogen, we are proud to offer our Capillary Sequencing Service (CES)—a precise and reliable solution for your sequencing needs. 🧬✨ Whether you’re a researcher or a clinician, our CES delivers the accuracy and detail necessary to drive breakthroughs in science and healthcare. With state-of-the-art technology and a commitment to fast, high-quality results, Macrogen is your trusted partner in advancing genomic research. Let us help you transform data into discoveries and insights into innovation. 🔬 Why Choose Macrogen CES? - Unmatched precision and accuracy - Fast and dependable service - A dedicated team focused on delivering the highest quality results Join us in advancing the future of genomics. Discover how Macrogen CES can empower your work and elevate your research. 🌍🔍 👉 Learn more: Order page: https://dna.macrogen.com/ Email: [email protected] #Genomics #CES #CapillarySequencing #Macrogen #InnovationInResearch

🔬✨ Don't Miss Our Exclusive Webinar Tomorrow! Join us tomorrow at 1:30 PM (Swiss time) for an in-depth webinar presented by our Ionic specialist, Michael Colombo. Discover how the Ionic system by Bionano is revolutionizing genomic research with isotachophoresis. Learn how to: - Achieve higher yields in DNA and RNA isolation - Implement simpler workflows to save valuable time - Reduce fragmentation for more reliable results This technology is a game-changer for anyone working with FFPE samples. Whether you're in biotech, life sciences, or genomic research, this webinar will provide invaluable insights to elevate your work. 🚀 Register now to secure your spot and stay ahead in your research: [https://lnkd.in/gfbSKhDu) ⏰ Hurry, registration closes soon! #GenomicResearch #DNAIsolation #RNAIsolation #Biotech #LifeSciences #ResearchInnovation #Webinar #FFPE #LabTech

Available in the BNLX and Nordics via BIOKÉ! 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

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

How to identify master regulators in signal transduction networks? What molecules might be responsible for gene up-regulation in your experiments? Just two steps could help to get the results, promoter analysis to identify TFBSs and then pathway analysis to compute master regulators.

Join us on June 18th at 6 PM CEST for the upcoming Coffee break with TRANSFAC devoted to the topic of pathway analysis and identification of master regulators.  Event details and joining link https://lnkd.in/eUqsKqSU In this webinar Dr. Alexander Kel, the CEO and CSO of geneXplain GmbH, will introduce you the Upstream Analysis approach that combines robust TRANSFAC TF binding site search with the fine pathway database TRANSPATH for reconstructing the key pathways and finding master regulators in them. You will learn how to use easy online tools that will automatically analyze your gene list, build specific gene regulatory and signal transduction pathway, find master regulators, and produce nice network visualizations ready for your paper. The following main questions will be in the focus of this seminar: Master regulators controlling the activity of transcription factors Walking pathways: pathway rewiring Integrated transcriptomics and proteomics analysis of Myc-induced U2OS cells (data from PMID: 26538417) Visualization of signalling pathways and networks #bioinformatics #SystemsBiology #geneXplain #TRANSFAC #TRANSPATH #HumanPSD #geneXplain_platform #CoffeeBreakWithTRANSFAC #GeneRegulation #Transcription #TranscriptionRegulation #TranscriptionFactors #Genes #research #Biology #PromoterAnalysis #TFBS #TranscriptionFactor #DNA #BindingMotif #PWM #PositionalWeightMatrix #TranscriptionFactorBindingSite #freeseminar #QandA #seminar #webinar #freewebinar #PathwayAnalysis #Pathways #MasterRegulator #MasterRegulators #Network #Networks #Reactome #KEGG #BioCyc

🔬✨ Happy National DNA Day! ✨🔬 Today, we celebrate the remarkable strides in understanding our genetic blueprint. At Avrok Bio, we're proud to be at the forefront of research utilizing DNA to unlock insights that drive innovation in healthcare and beyond. National DNA Day commemorates the completion of the Human Genome Project in 2003 and the discovery of DNA's double helix structure in 1953. It's a reminder of the immense potential within each strand of DNA and the limitless possibilities for improving human health and well-being. Our team is committed to harnessing the power of DNA sequencing and analysis to revolutionize personalized medicine, drug discovery, and agricultural biotechnology. Whether it's decoding rare diseases or optimizing crop yield through genomic selection, we're driven by our passion for scientific excellence and impact. Learn more about how Avrok can help get obtain DNA from your ideal patient population and turn those samples into relevant insights ➡️ https://avrokbio.com/ #CRO #TranslationalResearch #Biobank #ClinicalResearch #DNA #Sequencing #NationalDNADay #Genome #PatientCentricity