Pillar Biosciences Incorporated’s Post

🚀 Exciting Announcement! 🚀 Introducing a game-changing method now available on the Biomek NGeniuS system! This cutting-edge technology automates library preparation for the Pillar Biosciences oncoReveal™ Solid Tumor 22 Gene Panel, revolutionizing NGS workflows. Highlights: 🧬 Automated library prep for solid tumor samples, including both genomic and FFPE DNA. ⏱️ Streamlines labor-intensive manual steps, enhancing efficiency and reducing errors. 📊 Delivers high-quality sequencing data with Q30 scores >97% and on-target rates >92%. 💡 Ensures reproducible results with accurate variant detection and zero false positives/negatives. This innovation promises to revolutionize your lab's workflow, enabling consistent and high-quality results with minimal operator input. Explore how the Biomek NGeniuS system can transform your sequencing processes! #NGS #Automation #Biotech #Innovation #LabEfficiency

Finally, Pillar kit automated on Biomek NGeniuS !!

🔬 Thrilled to Present at SynBioBeta 2024! 🔬 Join Cedric Wu, VP of Innovation Center at GenScript USA Inc., on May 7th from 1:45 PM to 2:30 PM in the Grand Ballroom 220A for our session on "Accelerating Revolution in Biotech and BioPharma: The Power of Precision Mutant Libraries." 🧬 Discover the cutting-edge advancements in high-throughput DNA variant libraries that are reshaping protein engineering, target identification, and the development of gene and cell therapies. We'll explore how precision mutant DNA libraries, validated by deep learning models, are unlocking potential in areas like AAV capsids, enhancing tissue organ tropism, and CAR-T therapy design. 🌐 Whether you are involved in biopharma, bioengineering, or genomics, this session will provide a deep dive into the technologies driving rapid advancements in medical research and therapeutic development. Join us! https://lnkd.in/eWR-27hi #SynBioBeta2024 #Biopharma #GenScript #PrecisionHealth

We're excited to showcase our revolutionary PIPseq SEA Kit, which offers unparalleled stability for cDNA and enables researchers to delve into gene features and cellular functions without repeating experiments. This innovative tool is perfect for: 🔬 Deep re-sequencing after shallow screenings 🔬 Targeted enrichment of specific genes or features 🔬 Exploring cellular pathways in greater depth 🔬 Assessing specific molecules with custom DNA tags 🔬 Multi-omic analysis with other kits “One of the biggest challenges in using scRNAseq in drug development is assessing a single gene and its impact on the transcriptome. PIPseq’s SEA kit allows us to evaluate a specific target gene’s functional effect and its broader transcriptome impact in a single assay, seamlessly combining targeted assay specificity with the power of whole transcriptome analysis.” – Senior Scientist in Boston Biotech/Pharma Learn more about the SEA kit capabilities >> https://lnkd.in/gYuAdKdU

Discover the rising stars of nanotech, highlighting last year's emerging players: * Aera Therapeutics leads with breakthrough protein nanoparticle delivery technology, making genetic medicine more accessible. Its latest funding boosts efforts to tackle delivery hurdles and expand its applications. * Polyseql is transforming gene sequencing with its cutting-edge platform, accelerating the adoption of next-gen gene sequencers through recent investments. * Axoft pioneers in enhancing brain-machine interfaces with state-of-the-art implantable electronics, focusing on pre-clinical trials and scaling neural implant prototypes. These advancements reflect the sector's drive towards redefining healthcare, communication, and scientific discovery through nanotechnology. Stay tuned for more updates and insights in our upcoming posts. For a deeper dive into the industry, the full 2023 Advanced Technology Market Analysis report is available for download via the link in the comment section. #Nanotechnology #Innovation #TechTrends

🚀 **Unlocking the Future of Spatial Transcriptomics with SeekSpace®** 🚀 Despite significant advancements in resolution and throughput, RNA-permeabilization-based spatial technologies still face critical limitations, leading to challenges such as: 1️⃣ High cell heterogeneity in tissue sections and uneven permeabilization times. 2️⃣ Lateral diffusion of RNA during release, resulting in cross-contamination. 3️⃣ Inaccurate spatial cell mapping when integrating spatial and single-cell data. 4️⃣ Inability to obtain transcriptomic data and accurate spatial localization from the same cell. To overcome these technical hurdles, SeekGene has developed the groundbreaking spatial transcriptomics technology - **𝗦𝗲𝗲𝗸𝗦𝗽𝗮𝗰𝗲®**. SeekSpace® boasts true physical single-cell resolution, offering distinct technical advantages. It not only allows for precise cell type characterization but also enables accurate localization of cells and gene expression within complex tissue environments.🌍🔬 #SpatialTranscriptomics #SeekSpace #SingleCellResolution #ResearchInnovation #Biotechnology #GeneExpression #SeekingBiological

🚨 2023's Top Biotech Breakthroughs! 🚨 As we step into 2024, let's take a moment to reflect on the incredible strides made in biotechnology over the past year. My latest article dives into the Top Five Biotech Breakthroughs of 2023, showcasing innovations that have not just promised but delivered real-world impacts. From groundbreaking CRISPR-based gene therapies to AI's expanding role in drug discovery, these advancements are redefining healthcare and scientific exploration. 💡 Join me in exploring these pioneering technologies and their implications for our future. Plus, don't miss out on the honorable mentions that might shape the years to come. 👉 Read the full article here: https://lnkd.in/gsv4CxcM #biotechnology #innovation #healthcare #artificialintelligence #crispr #2023year

Oxford Nanopore Technologies and Twist Bioscience have partnered for a pharmacogenomics beta program. The program combines Twist's NGS reagents and enrichment panels with Oxford Nanopore’s sequencing platforms. The goal is to develop long-read PGx workflows for personalized medicine. These workflows provide genetic results in a single end-to-end process, eliminating the need for follow-up testing. The beta program has already resolved the CYP2D6 gene in one assay. Twist’s hybrid capture panels will also be compatible with Oxford Nanopore's platforms. Twist CEO Emily Leproust highlighted the collaboration's potential for personalized therapies. Oxford Nanopore CEO Gordon Sanghera emphasized the benefits of their technology for comprehensive genetic analysis. #pharmacogenomics #personalizedmedicine #NGS #genetics #research #biotech #sequencing #genomics #collaboration #innovation

🚀 What's going on in the Single-cell Omics Market? 🚀 The global single-cell omics market is set to skyrocket, reaching an impressive valuation of $35.11 billion by 2033, up from $4.16 billion in 2023. This rapid growth, driven by advancements in high-throughput sequencing and increased demand for personalized medicine, highlights the pivotal role of single-cell analysis in understanding cellular processes and disease mechanisms. So who are the contributors? 10x Genomics brings key innovations including the Visium HD platform offering higher resolution spatial transcriptomics, the Xenium In Situ platform with multimodal cell segmentation and expanded gene panels. The next-generation Chromium GEM-X platform improves gene detection, cell throughput, and cost efficiency. Vizgen's new MERSCOPE Ultra Platform and MERFISH 2.0 chemistry, introduced at AACR 2024, enhance single-cell spatial transcriptomics. The Ultra Platform triples the imaging area and doubles the speed, boosting sample flexibility and throughput. Mission Bio reveals the Tapestri Platform. The first single-cell technology was developed to uncover biomarkers that help stratify patients, signal resistance, and predict relapse. Tapestri's powerful multi-omics capability connecting genotype and phenotype; opens the door to a deeper understanding and improved treatment of cancer. The development of this new technology paves the way for further single-cell analysis, contributing to the overall treatment of our well-being and healthcare across the world. Who else will be contributing to new single-cell technology this year? #biotech #singlecellomics #genomics #innovation #healthcare

Our NGS #DxBooks are updated quarterly with new insights into changes in the sequencing competitive landscape. Using our proprietary licensable data, our NGS Dx Books expert Rishikesh Kayathi conducted an analysis comparing Illumina and Thermo Fisher Scientific platforms and assays in clinical #oncology and observed three notable trends since last year: Diversity and Dominance in Gene Panels Illumina leads in panel diversity and volume, leveraging an expansive range of third-party kits. Our data visualizes this dominance across various panel sizes including WES and WGS, and the impressive traction these approaches have gained in recent years. Regional Dynamics and Market Shares While ThermoFisher has carved a niche in smaller gene panels (1-52 genes), especially in Europe, Illumina continues to expand its footprint in larger panels, with a dominant position in the U.S. Strategic Positions in a Competitive Field Despite challenges in the stock market, Illumina's strategic partnerships with reagent and bioinformatics firms like Pillar Biosciences Incorporated and Velsera has solidified its entrenched market position, simplifying workflows and enhancing user experiences. Conversely, ThermoFisher’s investment in an integrated ecosystem with solutions like Ion Chef and Ion Reporter caters to labs seeking end-to-end automation. Interested in deeper dive? Request a demo or sample of our data here: https://lnkd.in/e-w5Q5HX