DISPENDIX’s Post

Enhance a wide range of analytical and diagnostic workflows with our Pre-configured Genomics Content Package! Built with 64 pre‑configured techniques that support the standard analytical workflows used by typical #genomics lab, providing you with comprehensive coverage. See what else is included in our latest #CLS Pre-configured Content Package! Download full infographic here https://lnkd.in/erfMKn_E #Clinisyslaboratorysolution #LIS *Clinisys™ Genomics Laboratory and the Pre-configured Genomics Content Package are available exclusively in North America.

How do you read something as microscopic as DNA? 🧬 With sequencing by expansion (SBX) we’re setting a new standard for what next-generation sequencing can achieve. Instead of trying to shrink our "cameras", #SBX technology uses a radical idea: it expands the DNA. The process creates a synthetic copy called an Xpandomer, which is 50 times longer than the original molecule. This expansion spaces out the "letters," making them clear and easy to read as they pass through a tiny pore. Watch the full video (link in comments) to explore the potential of SBX and how it differs from other technology. #Genomics #InnovatingDiagnostics #NGS

The field of genomics is evolving, and sequencing by expansion (SBX) is designed to be at the forefront of this transformation. Designed to deliver full-length reads in seconds, SBX will power faster insights and open up new possibilities for genomics. Whether it’s accelerating innovation or pushing the boundaries of scientific discovery, SBX is being designed to set a new standard for what next-generation sequencing can achieve. Watch the full video to explore the potential of SBX and how it differs from other technology: https://spkl.io/6042AA00k #Genomics #HumanGenetics #RocheSBX #Innovation #NGS

Transform your lab’s throughput and consistency. High-throughput workflows demand more than speed — they demand reliability at scale. The Turbo Grinder enables labs to process up to 576 samples in a single run, delivering uniform, high-quality homogenisation across every well. That means: - More consistent downstream results - Smoother integration with automated pipetting systems - Reduced variability across high-throughput assays - Significant time and labour savings By standardising sample disruption, you create a reliable foundation for accurate, scalable analysis — whether in genotyping, genomics or broader molecular workflows. https://lnkd.in/eVRh9MSw #Genotyping #LabAutomation #HighThroughput #MolecularBiology #Genomics #PCR #LifeSciences #MakingScienceAffordable

Advanced Genomic Services I Stories From Our Annual Report What happens when genomics moves beyond standard sequencing to truly bespoke, precision‑driven solutions? What new insights emerge when we can see not just DNA sequences, but how the genome folds and interacts in three dimensions? What hidden biology is revealed when we study disease, development and treatment response one cell at a time? At AGRF, these questions sit at the heart of our Advanced Genomic Services (AGS). Built within our Innovation & Development framework, AGS brings together cutting‑edge platforms, custom assay design and deep scientific expertise to support researchers tackling the most complex biological challenges. From 3D genomics and single‑cell sequencing to advanced chromatin mapping, AGS is helping enable next‑generation discovery and turning curiosity into meaningful scientific impact. Pictured: Mary Matthews, PhD, Peter Lau and Dhanya Sooraj 🔗 Read the full story in our Annual Report, P26: https://lnkd.in/gPB_QJFd #AnnualReport #AdvancedGenomicServices #Innovation #SingleCell #3DGenomics #Research #Genomics

Proud to be featured in this year’s Annual Report and to work alongside the incredible team behind AGRF's Advanced Genomic Services. AGS truly sets the benchmark for bespoke, precision driven genomics, combining world class platforms, deep scientific expertise and genuine collaboration to help researchers tackle the most complex biological questions. From single cell sequencing to 3D genomics and advanced chromatin mapping, AGS consistently goes beyond standard sequencing to deliver meaningful scientific impact. An amazing example of innovation in action and genomics done right. #AGRF #AdvancedGenomicServices #AGS #Genomics #Innovation #SingleCell #3DGenomics #Research #AnnualReport

Excited to collaborate with the Canada's Michael Smith Genome Sciences Centre to bring single cell Flex Apex to the GSC community! 🚀 As single-cell becomes the standard, transitioning from bulk RNA-seq is no longer a question of *if* it's *how*. That's where Flex Apex from 10x Genomics comes in, enabling high-sample, cost-effective studies across diverse sample types. This workshop is a fantastic entry point for anyone looking to: ✅ Understand best practices for experimental design ✅ Make the leap from bulk to single-cell ✅ Leverage Flex Apex for scalable, high-throughput studies 📅 May 21, 2026 | 9:00–10:30 AM PT 📍 In person at the GSC (Vancouver) + virtual option Expanding access to single-cell capabilities, especially for bulk users. 👉 Register here: https://10xgen.com/1Zh #SingleCell #Genomics #scRNAseq #GSC #ResearchEvents #Partnership

💫 We are delighted to share that our upcoming #MVIF 49 event is supported by INTEGRA Biosciences. As part of the programme, we will be hosting Dr. Dagmara Lewandowska, who will present their work on reliable and cost-effective NGS library preparation using INTEGRA's MAGFLO™ NGS magnetic beads for Illumina MiSeq amplicon sequencing. 🗒️ Her talk draws on a rigorous comparison between MAGFLO NGS and other gold standard magnetic beads in 16S rRNA and ITS amplicon sequencing workflows, demonstrating equivalent performance and no sequencing bias in microbial diversity analysis. A valuable contribution for anyone working in genomics or microbiome research and looking for a room temperature stable magnetic beads. Check out the full programme and registration details: https://lnkd.in/dw-wyj-p

I recently received a question from a graduate student asking which integration strategy to use in a multi-omics study. Here is a concise answer for anyone navigating the same decision. Three integration strategies in multi-omics Early integration ·  Concatenate all omics layers before modelling ·  Best for: broad molecular discovery in well-harmonized cohorts Intermediate integration ·  Learn a joint latent space across layers before inference ·  Best for: patient subtyping and stratification Late integration ·  Model each layer independently, then combine outputs at the decision stage ·  Best for: real-world deployment with incomplete patient profiles #MultiOmics #Bioinformatics #PrecisionMedicine #ComputationalBiology #Genomics #DataScience #Biostatistics

Some of our talented colleagues during their talk today at the #genomicsshowcase2026 - 'A look into the All Wales Medical Genomics Lab : from DNA to data' - the team gave insight into the processes behind the scenes, covering everything from DNA sample processing to interpreting the data collected. We hope you enjoyed this insight into the world of AWMGS labs, and look forward to sharing more information like this on our channels in the future 🧬 🏴󠁧󠁢󠁷󠁬󠁳󠁿 #dna #bioinformatics #geneticcounselling #welshgenomics