BioDock’s Post

Unlock the power of #single-cell #multiomics with the 10x Genomics #Chromium platform: achieve high-quality #transcriptome data, recover more cells, and maximize insights while reducing hidden costs. Discover more with less effort and elevate your research to new heights.

good opportunity

Only one week to go until our webinar with Pacbio expert Thea Zieglar on “Long-read sequencing, the next era of genomics”. Join Thea and Novogene Deputy Director of Product Marketing, Shi-qi Ann as they guide you through the principles and advantages of highly accurate long-read sequencing with the PacBio Revio. In this webinar we will present new trends in the genomics field as well as an overview of major applications. The new Kinnex applications increase throughput for full-length RNA, single-cell RNA, and 16S sequencing on PacBio long-read sequencing systems to enable large-scale studies at extraordinary resolution. Key takeaways: • Understand the principle and advantages of highly accurate long-read sequencing to explore the full spectrum of genetic variation • Gain an overview of the most important applications, including whole genome sequencing, targeted sequencing, RNA sequencing and microbial genomics • Understand how PacBio long-read sequencing of extended 16S amplicons enables identification of metagenome community members at higher taxonomic resolution than common methods • Learn how Kinnex full-length RNA and single-cell RNA sequencing enables scientists to capture full-length isoforms, elucidating isoform diversity in development and disease Webinar date: 10am BST/11am CEST Tuesday 23rd July 2024. Register here: https://bit.ly/3VUk2Ow #LongReadSequencing #PacBioRevio #WholeGenomeSequencing #RNASequencing

What is it like to work in DNA sequencing? Read our blog to find out what a day in the Genomics facility involves: https://lnkd.in/eVdMWN_r #DNADay

Having worked with MinION in the lab setting and analyzing Long read Data, here is a short summary of the technology.

Illumina sequencing revolutionizes the field of genomics with its high-throughput, precise, and efficient approach to DNA sequencing. By leveraging reversible dye terminators, this method allows for the simultaneous sequencing of millions of DNA fragments. Here's how it works: DNA samples are fragmented, and adapters are attached to create a library. These fragments are then amplified on a flow cell, forming clusters. Sequencing occurs as fluorescently labeled nucleotides are incorporated one by one, and a camera captures the emitted light to identify each base. This cycle repeats, generating vast amounts of data that can be analyzed to unlock the secrets of our genetic code. #Genomics #IlluminaSequencing #DNA #Biotech #ScienceExplained 🧬✨

🌟 Discover the World of 3D Genomics! 🌟 Join us for an insightful webinar, “3D Genomics 101,” where we’ll introduce the what, why, and how of 3D genomics. The webinar will cover: 🔹 The role of 3D genomics in research 🔹 Methods used to study 3D genomic structures 🔹 Techniques for data visualization 🔹 Real-world case studies 🔹 How to access 3D genomics with Dovetail® Assays 🔹 What sets Dovetail® apart This is a must-attend event for researchers and professionals looking to deepen their understanding of 3D genomic techniques and tools! 🗓️ Date & Time: Thursday, October 3rd at 8:30 am PDT 🔗 Sign up here: https://ow.ly/6GKt50Tyvqr Don’t miss out on this opportunity to explore the cutting edge of genomics with Dovetail! #GenomicsWebinar #3DGenomics #DovetailGenomics #Bioinformatics #3DGenomics, #Hi-C, #Chromatin

Considering #epigenetic & #Chromatin #research? Want to learn about #3Dgenomics? Dovetail Genomics provide the best tools for your research questions. Join Mia Truong for an insightful webinar!

🚀 Introducing MEGAnnotator2: A Next-Level Genome Annotation Pipeline 🧬 Unlock the power of modern sequencing technologies with MEGAnnotator2, a fully automated, user-friendly bioinformatics pipeline designed to handle both short- and long-read DNA sequences. It delivers high-quality microbial genome assemblies and functional gene annotations—without requiring extensive bioinformatics expertise. Key points include: 🧬 Supports all next-gen sequencing formats (short/long reads). ⚡ 43x faster execution time than the previous version. 📊 Provides comprehensive reports on genome features and statistics. 💡 New features: DNA quality check, metabolic profiling, modular architecture for easy customization. 💾 80x reduction in database storage requirements. MEGAnnotator2 empowers researchers to streamline microbial genome reconstruction and functional analysis with ease! #Bioinformatics #Genomics #DNASequencing #Microbiome #NGS #GenomeAnnotation #DataScience Details：https://lnkd.in/gGUaHeAX

𝗘𝗹𝗲𝘃𝗮𝘁𝗲 𝗬𝗼𝘂𝗿 𝗡𝗚𝗦 𝗟𝗶𝗯𝗿𝗮𝗿𝘆 𝗣𝗿𝗲𝗽 𝘄𝗶𝘁𝗵 𝗖𝗹𝗲𝗮𝗻𝗣𝗹𝗲𝘅 𝗧𝗲𝗰𝗵𝗻𝗼𝗹𝗼𝗴𝘆 Say goodbye to complex workflows—Paragon Genomics' CleanPlex technology simplifies NGS library preparation into just 3 steps, completed in about 3 hours: 1️⃣ 𝗠𝘂𝗹𝘁𝗶𝗽𝗹𝗲𝘅 𝗣𝗖𝗥: Amplifies target regions with precision using our proprietary ParagonDesigner™ algorithm for high specificity. 2️⃣ 𝗕𝗮𝗰𝗸𝗴𝗿𝗼𝘂𝗻𝗱 𝗖𝗹𝗲𝗮𝗻𝗶𝗻𝗴: Removes non-specific PCR products, like primer-dimers, ensuring only your sequences of interest are retained. 3️⃣ 𝗜𝗻𝗱𝗲𝘅𝗶𝗻𝗴 𝗣𝗖𝗥: Barcodes your libraries with platform-specific indexes, ready for sequencing on Illumina, Ion Torrent, and more. Achieve exceptional data quality, efficient use of sequencing reads, and accurate variant detection—even with degraded samples. Paragon Genomics #Cleanlex #NGS #Libraryprep #Genomics #Paragonenomics #Precisionscience