BioSkryb Genomics

Available now! New user guides enable hybrid capture downstream of ResolveDNA® and ResolveOME™ Single-Cell Core Kits, allowing researchers to perform whole exome or targeted panel sequencing at single-cell resolution. Contact us to request your user guide copies! https://lnkd.in/eSUzQtNM #WholeExomeSequencing #SingleCell #Genomics #Multiomics

New Preprint Alert! Read how Zhou et al. used single-cell sequencing methods, including ResolveDNA® whole genome amplification, to better understand the pathogenesis of neurodegenerative disorders. https://lnkd.in/g6A6U42k #genomics #singlecell #neurodegenerativeresearch

Our Certified Service Provider (CSP) Program offers the full range of BioSkryb ResolveServices℠, delivered through our partner labs. CSP status ensures that our partners provide the same precision and expertise as BioSkryb’s in-house services, with added benefits such as expanded sequencing options, adjacent technologies, and CAP/CLIA certified labs for regulated work. Each CSP undergoes rigorous training and validation by BioSkryb’s ResolveServices team to maintain the highest standards of performance and accuracy. To see a list of our current CSP Program members, visit: https://lnkd.in/gbjCA2N3 To learn more about ResolveServices, visit: https://lnkd.in/emA8qnmg

ResolveSEQ MRD, is an innovative ResolveServices℠ offering designed to empower further classification and characterization of the measurable residual disease (MRD) cells in hematologic malignancies. If you are interested in implementing the ResolveSEQ MRD workflow into your own laboratory, contact us today: https://lnkd.in/eSUzQtNM Read more about ResolveSEQ MRD: https://lnkd.in/gw6c78Ny

Did you miss BioSkryb’s latest poster at #AGBTGM? Check out the “A high-plexity exome solution tailored for sensitive variant detection in single cells” poster on our website now: https://lnkd.in/gZyiFBdJ Looking to access our dedicated protocols for generating libraries compatible with hybridization capture? Connect with our FAS team to get your copy today https://lnkd.in/eSUzQtNM   #genomics #multiomics #singlecell #exome

Our BaseJumper® bioinformatics platform includes demo data from ResolveDNA® and ResolveOME™ products. Explore the data today: https://lnkd.in/grSG5P4b Want to learn more about the three different options for using BaseJumper in your research? Learn more: https://lnkd.in/gedRfE4X #genomics #multiomics #singlecell

We are happy to announce new user guides that enable hybrid capture downstream of ResolveDNA® and ResolveOME™ Single-Cell Core Kits, allowing researchers to perform whole exome or targeted panel sequencing at single-cell resolution! Features include: 🧬 Libraries with DNA fragment lengths ideal for hybrid capture 🧬 Produces a pool of up to 96 single-cell genomic libraries ready for hybrid capture 🧬 Compatible with third-party hybrid capture kits and protocols Contact us to request your user guide copies! https://lnkd.in/eSUzQtNM #WholeExomeSequencing #SingleCell #Genomics #Multiomics

Are you looking for a way to amplify genomic DNA from low input samples? Primary template-directed amplification (PTA), first described by Gonzalez-Pena et al. (PNAS 2021), provides superior genomic coverage and allelic balance compared to other whole genome amplification methods. PTA is found in all BioSkryb Genomics products, including the ResolveDNA® Whole Genome Amplification Kit, which features the power of PTA with flexibility in downstream applications, from PCR to next-generation sequencing. Learn more:  https://lnkd.in/gpDP_Vwz #genomics #lowinput #wholegenomeamplification

Next week, Victor Weigman will be representing BioSkryb at the AGBT - Advances in Genome Biology and Technology annual meeting. Connect with him at his poster on Monday, February 24th during the Coffee and Dessert poster session or schedule some time during the conference! https://lnkd.in/g_6Qk4bX   #genomics #multiomics #singlecell

The ResolveOME™ Whole Genome and Transcriptome Single-Cell Core Kit couples BioSkryb’s whole genome amplification chemistry, primary template-directed amplification (PTA) first described by Gonzalez-Pena et al. (PNAS 2021), with a whole transcriptome assay. The core kit features an eight-hour workflow, including all the reagents needed to take you from cells to sequencing-ready libraries. Our single cell core kit enables you to:  🧬 Integrate DNA+RNA data from every cell 🧬 Study impact of somatic mutations on gene expression 🧬 Generate libraries from single cells in under 8 hours Learn more: https://lnkd.in/gNSzPSEK #genomics #multiomics #singlecell