BGI Genomics的动态

Unlock the secrets of chromatin! ?? Eurofins Genomics proudly introduces MNase Sequencing, a revolutionary method revealing chromatin structures and nucleosome positioning. Empowering researchers with innovation for genomic excellence. ?? Learn more: [https://lnkd.in/gPs7UgZx) #MNaseSequencing #ChromatinResearch #GenomicsInnovation #EurofinsGenomics #NucleosomePositioning

Will you be at #SLAS, Boston? Stop by the poster 1232-A, Automating PacBio? SMRTbell? Prep Kit 3.0 workflow on the Revvity Sciclone? NGSx G3 Workstation and gain insights on long read sequencing and how to generate whole genome sequencing (WGS) libraries. For research use only. Not for use in diagnostic procedures. https://ms.spr.ly/6042ivoKs

Happy to share that our paper on V-pipe 3.0 is out now! V-pipe 3.0 is a computational pipeline specifically designed for analyzing short viral genomes using next-generation sequencing data. V-pipe 3.0 enables sustainable viral genomic data science. You can check out the published paper of our work in GigaScience. The link is in the first comment. It has been great learning and collaborating with you, Kim Philipp Jablonski and Ivan Topolsky! #computationalbiology #bioinformatics #nextgenerationsequencing #highperformancecomputing #virusevolution

Really exciting to see the launch of this new consortium - Impact of Genomic Variation on Function (IGVF) ?? The goal is to create a mechanistic map translating human genetic variants to cellular function, in an open resource for the community. I'm confident it will have big impact on the future of the field. It is efforts like these we need to push drug discovery to the next level. ?? Read the publication here: https://lnkd.in/ddxpp7mN Authored by an all star team of researchers from top institutions like Broad Institute of MIT and Harvard and Stanford University, including Bradley Bernstein, Jason Buenrostro, Luca Pinello, Jesse Engreitz, Anne Carpenter, ANSHUL KUNDAJE, Jay Shendure #DrugDiscovery #TargetDiscovery #Genomics

?? As this interesting article from Genomics England shows, previously classified genetic variants play a crucial role in future diagnostics. So how does your lab ensure that past classifications are accessible and useful? With AION - our AI-driven variant interpretation solution - our manual variant classification feature allows scientists to store, find and revisit previous classifications. This provides a foundation for faster, more accurate diagnoses, saving time while ensuring consistency across teams. ?? https://lnkd.in/eFFqwHJy Learn more about how AION can bring speed and efficiency to your workflow. Book a demo with our team! https://lnkd.in/eTNR8S8u #Genomics #AION #PrecisionMedicine #VariantClassification #ClinicalDiagnostics #Bioinformatics

Reveal more for less with groundbreaking savings on #Revio system. Rev up your research with Revio system, designed for high-throughput studies so that you can see all types of genomic variation — from small to large — all in one go. For a limited time, bring HiFi sequencing to your team at ~50% the upfront cost. See how: https://bit.ly/43x6yLL #PacBio

Our latest blog post dives deep into the revolutionary chemagic 360 instrument. Dr. Karine Auribault shares her insights on how this cutting-edge technology is transforming genetic testing. From high-quality DNA extraction to downstream applications like Next Generation Sequencing and digital PCR, the chemagic 360 is a game-changer. Read the full post to stay ahead in the field of genetic research! https://ms.spr.ly/6041lVFLJ For research use only. Not for use in diagnostic procedures. #GeneticTesting #DNA #Revvity #chemagic #NucleicAcidPurification

Recently, we had the pleasure of presenting a poster created in collaboration with Genomics England, authored by Luke Paul Buttigieg and B?a?ej Szczerba: "How we’re revolutionizing Genomics England’s clinical data processing pipelines, and how you can leverage our learnings in your research." The poster focuses on migrating clinical genetic diagnostics services to Nextflow, enhancing reliability and supporting novel use cases. This transition aims to improve clinical services and increase research data generation. If you are interested in these topics, here is the link to the poster: https://lnkd.in/dqRDCeYv If you would like to learn more, feel free to reach out to the poster's authors. #Genomics #GeneticDiagnostics #Nextflow #ClinicalResearch

Elevate your research with Source Genomics reliable qPCR services ?? Are you looking to accurately measure DNA or RNA levels in your samples with unparalleled precision and efficiency? Source Genomics offers cutting-edge qPCR services designed to meet your research needs. Contact us today for more information ?? https://lnkd.in/eGP2B6P9 #Genomics #SangerSequencing #NGS #Sequencing #GenomeMapping #Biomarkers #BiomarkerDiscovery #Multiomics #DrugDiscovery #qPCR #TheSequencingPeople #Science #LifeScience

?? Thrilled to share our latest blog post focusing on the crucial topic of minimizing index hopping in next-generation sequencing (NGS) technology! Dive into the details here: How to Prevent Index Hopping: https://lnkd.in/gTGqVR8d In the realm of genomics, where accuracy is everything, understanding and mitigating index hopping are essential. Our blog post delves into the complexities of this phenomenon and offers actionable strategies to safeguard your sequencing data. Learn about the factors contributing to index hopping, such as residual adapters and index primer oligos, and discover effective techniques like Unique Dual Index (UDI) to ensure data integrity. Whether you're performing germline variant analyses or exploring somatic variant detection, mastering the prevention of index hopping is crucial for reliable results. Check out our blog post now to streamline your sequencing workflow! #NGS #Genomics #IndexHopping #SequencingData #UDI #ClinicalLaboratories #DataIntegrity #Ngspanel