SPT Labtech’s Post

BioSkryb Genomics is proud to announce our new ResolveDNA® Whole Genome Single-Cell Core Kit is now shipping. The ResolveDNA Core Kit combines the power of primary template-directed amplification (PTA) with library preparation and adapter ligation to provide a convenient, scalable, and streamlined workflow, while maintaining industry-leading whole genome amplification. Additional details on this new product, including performance specifications, can be found in the product brochure: https://lnkd.in/ePiJPb4R ResolveDNA can help you: • Capture 97% of the genome • Analyze co-occurring SNVs, CNVs, and SVs • Resolve clonal architecture with unprecedented resolution Learn more: https://lnkd.in/dwUxZqV5 #genomics #multiomics #singlecell

Did you know that not all companies who provide sequencing services are equal in their offering? Furthermore, failing to have the right considerations in place before working with them can result in a loss of time, expenditure, and precious samples. At Sampled, our experts collaborate with clients to ensure that the right platforms and experimental designs are selected based on their specific needs. Learn more about the four key considerations before outsourcing your samples for RNA-Sequencing by checking out our article here: https://bit.ly/48ubjqW #Sampled #rna #rnaseq 10x Genomics #sequencing

The field of NGS analysis is rapid evolving. Delve into the latest advancements in sequencing analysis from Illumina through collaborations with leading institutions such as Baylor College of Medicine. Learn more about the latest innovations from Illumina informatics, including the newest versions of DRAGEN and Genomic AI tools that are pushing the boundaries of genomic analysis. #ngs #sequencing #wgs #bioinformatics #DRAGEN #genomicAI

Now with more content! Come learn how to improve your single cell workflow this Tuesday.

January 2024, our method HAT for calling de novo variants published now in Bioinformatics at https://lnkd.in/gcKxBf5D. This is @TNTurnerLab paper#8 #bioinformatics #denovo #genomics #genetics

#Advances and #Trends in #OmicsTechnology Development The human history has witnessed the rapid development of technologies such as #highthroughput #sequencing and #massspectrometry that led to the concept of “omics” and methodological advancement in systematically interrogating a #cellularsystem. Yet, the ever-growing types of #molecules and #regulatorymechanisms being discovered have been persistently transforming our understandings on the #cellularmachinery. This renders cell omics seemingly, like the universe, expand with no limit and our goal toward the complete harness of the cellular system merely impossible. Therefore, it is imperative to #review what has been done and is being done to predict what can be done toward the #translation of omics information to disease control with minimal cell perturbation. With a focus on the “four big omics,” i.e., #genomics, #transcriptomics, #proteomics, #metabolomics, the authors delineate hierarchies of these omics together with their epiomics and interactomics, and review technologies developed for interrogation. Edited by Roberto Gramignoli

🔬🚀 "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

Did you know our DNA sequencing team offers a genomic consulting service through QIB Extra?🧬 Our methodology extends beyond just generating sequencing data. We incorporate a robust bioinformatics pipeline for data processing, alignment, and analysis, ensuring precision at every step. By employing variant annotation, we add functional insights to identified variants, providing deeper understanding. Moreover, our integration of both short- and long- read data guarantees a comprehensive genomic analysis. Find out more ➡️ https://buff.ly/45m0XsA #DNASequencing #Biotech #Genomics

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