Enhanced my skills in genomics research and biotech advancements through a hands-on course, mastering multiple sequence alignment, variant study, and phylogenetic analysis. Equipped to drive innovation in genomics and biotech applications. Open to exciting opportunities in this field! #Genomachub #GenomicsCourse #BiotechAdvancements #GenomicEvolution #MultipleSequenceAlignment #PhylogeneticAnalysis #GenomicsResearch #BiotechCareers #GenomicsInnovation"
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Third-generation sequencing, also referred to as long-read sequencing, represents a category of DNA sequencing techniques that generate lengthier sequence reads. In comparison to second-generation sequencing, commonly known as next-generation sequencing, third-generation sequencing technologies have the capacity to produce significantly longer reads. This characteristic bears significant implications for genome science and broader biological studies. Who invented this and when? Third-generation sequencing was developed by Pacific Biosciences (PacBio) and Oxford Nanopore Technology (ONT) and has been under active development since 2008. What are the companies leveraging it? Some big names that are leveraging this innovation are Pacific Biosciences of California, Genia Technologies, Stratos Genomics, GATC Biotech AG, Phase Genomics, and Loop Genomics. #BioAngelsBiotechChronicles #BioAngels #HealthcareInnovations #HealthcareSolutions
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We’re paving the way through our collaboration with CiberMed to enable a new Targeted Digital Cytometry method from bulk RNASeq data! If you are doing immune cell profiling but need a way to scale your sample numbers or address tissue dissociation bias, this method might be for you! #targetenrichment #digitalcellprofiling #cellprofiling #immunecellprofiling #deconvolution #rnaseq #cibermed
🔎Unveil a significant advancement in genomics research with Agilent SureSelect RNA-Seq, paired with iSort digital cytometry from CiberMed. This technology offers unparalleled accuracy in cell type profiling with 20x less sequencing than traditional methods. Developed with the expertise of CiberMed and Stanford University, it’s set to transform research by providing a robust, efficient, and precise solution for analyzing cell type compositions in solid tissue samples.💡 👨🔬Explore how this innovative approach can elevate your research capabilities. Dive into the detailed study to see the future of genomics. Agilent Technologies #Genomics #Innovation #Research #CiberMed #StanfordUniversity #RNASequencing #Biotech
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🟣 Business Development Manager at GeneTiCA group | Executing your complex solutions in Multi-Omics & NGS | Driving Innovation | Biotechnology and Automation | Medical and Diagnostics technology
🔬🚀 "Innovation is like a speeding train – it keeps accelerating!" 🚀🔬 Just look at the journey of genomic technology. In 2013, sequencing a human genome cost $5,467. Fast forward to 2023, and it’s now just $𝟐𝟎𝟎 𝐩𝐞𝐫 𝐠𝐞𝐧𝐨𝐦𝐞 - a staggering 96% decrease! 📉 To put that into perspective, you can now sequence your own genome for the price of a new pair of quality shoes! This incredible progress highlights the rapid advancements in genomic technology. As biotech enthusiast, it's thrilling to see how accessible and efficient genome sequencing has become. These advancements are paving the way for exciting new possibilities in research and personalized medicine. If you’re as fascinated by this and want to dive deeper into the world of genomics, check out our work at GeneTiCA Group by visiting our website at https://www.genetica.cz/ #Genomics #Innovation #Biotechnology #GenomeSequencing #TechAdvancement #GeneTiCA #GetToKnow
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Here at the #LorneCancer conference. Come visit our booth, and talk to us on how we can help with your Cell Biology, Genomics and Drug Discovery workflows. #Tecan
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🧬 New Developments in Single-Cell Transcriptomics! 📊 A recent study by Lucas Kuijpers and colleagues, published in BMC Genomics, evaluates into the efficiency of various bioinformatic pipelines for SPLiT-seq, a different approach for single-cell transcriptome sequencing. 🛠️ SPLiT-seq is a single-cell transcriptome sequencing technique that uses a combinatorial barcoding approach by splitting and pooling cells into multi-well plates with barcodes, recently commercialized by Parse Biosciences 📊 Evaluated pipelines include STARsolo, splitpipe, and alevin-fry splitp among others, highlighting their ability to handle large datasets effectively 🔎 While STARsolo and splitpipe are recommended, STARsolo requires additional coding. 📚 BMC paper: https://lnkd.in/dzaw--qB 👩💻 STARsolo: https://lnkd.in/d2vmaDPG 👩💻 splitpipe: https://lnkd.in/dxnFgbPs 📢 Join the Conversation 📢 Share your ideas, methods, and tools in the comments! 👇 💬 #Genomics #Bioinformatics #Transcriptomics #Biotechnology #SPLiTseq
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Data Operations Lead AstraZeneca | PhD Cheminformatics - National University of Singapore | Former Scientist @ University of Cambridge, CRUK-MI and ICR- Oslo | Computational Biology | AI-driven Drug Discovery
good opportunity
Great opportunity to learn about single cell genomics!
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Working with Tissue DNA Isolation optimization... Formulation of Enhanced Lysis Buffers... Good Laboratory Practices Research and Development VETA Genomics . #molecularbiology #genomics #researchanddevelopment #validation #dna #moleculargenetics #biotechnology
Validating MACHEREY-NAGEL Tissue DNA Isolation kit with Enhanced Tissue Lysis Buffer Formulated by VETA Genomics - R&D Veta Genomics Team #molecular #vetagenomics #validation
Tissue DNA Extraction At Veta Genomics
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What could you discover with highly accurate long-read sequencing at scale? The submission window is now open for the 2024 Microbial Genomics SMRT Grant. Tell us in 100 words or less how HiFi sequencing will advance your microbiome and metagenomics research for a chance to win free sequencing! Details on how to apply: https://bit.ly/3z89XFJ #PacBio #Metagenomics #MicrobialGenomics
2024 PacBio SMRT Grant | Microbial
programs.pacb.com
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[𝗠𝗲𝗲𝘁 𝘁𝗵𝗲 𝘀𝗰𝗶𝗲𝗻𝗰𝗲] Did you know that the discovery of the double helix structure of DNA 🧬 by James Watson and Francis Crick in 1953 revolutionized the field of molecular biology? It provided a deeper understanding of how genes control cellular processes and led to groundbreaking insights into the genetic code and protein synthesis. This discovery also paved the way for the development of the #biotechnology industry. One of our common priorities is to develop #genetherapies that have the potential to positively impact the lives of the patients and families devastated by rare and life-threatening genetic diseases. At Novartis, we are enthusiastic about the science behind our work, breaking barriers, and finding answers to difficult questions. #reimaginingmedicine #innovation #DNA #science
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🔬 New Technology for Spatial Genomics! 🧬 Check out the recent study "Slide-tags enables single-nucleus barcoding for multimodal spatial genomics" published in Nature by Andrew J. C. Russell et al. 🚀 Slide-tags allows tagging single nuclei within intact tissue sections using spatial barcode oligonucleotides from DNA-barcoded beads with less than 10 μm spatial resolution and high-quality whole-transcriptome data. 🧫📊 🔵 Adaptable to various single-cell measurement technologies, including multiomic measurements of open chromatin, RNA, and TCR sequences. 🟠 Successfully used in the human cortex to uncover cell-type-specific spatial gene expression patterns and identify spatially varying genes systematically. 🟣 Analyzed densely packed tissues like the human tonsil, identifying subpopulations and spatially varying genes in germinal center B cells, T follicular helper cells, and follicular dendritic cells. 🟢 Achieved higher spatial resolution and molecular sensitivity compared to existing approaches. 📚 Nature paper: https://buff.ly/3RnwqUR 📢 Join the Conversation 📢 Share your ideas, methods, and tools in the comments! 👇 💬 #Genomics #SpatialGenomics #SingleCell #Bioinformatics #Pharma #ResearchInnovation #Biotechnology #LifeSciences #NatureResearch
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