Lexogen’s Post

🔬 Say hello to Live-seq, the cool new scRNA-seq method that lets us spy on cellular secrets over time! By taking tiny cytoplasmic biopsies from living cells, we can sample the SAME cell again and again. 💡 And when we team up Live-seq with Lexogen's #LUTHOR HD kit, we’re supercharging our gene detection from 1000-1500 genes to a whole new level, opening up amazing new possibilities in biomedical research. 😎  Check out Lexogen's article below and our blog post "LUTHOR HD: Pushing the Boundaries of Single Cell Transcriptome Analysis" https://lnkd.in/gMa93g8f

Single-cell RNA sequencing and single-nucleus RNA sequencing are efficient approaches for studying transcriptomes. Discover the advantages and applications of these powerful tools to determine which one fits your research needs. https://lnkd.in/g-d2bFK5

Join Nan Fang at the prestigious #GRC meetings to discuss our poster: 📣 Simultaneous single-cell genome and transcriptome sequencing at scale. Our AccuraSCOPE® Single Cell Transcriptome and Genome Library Kit may be your answer if your next project needs single-cell sequencing for both! Learn more about opening up new possibilities for single cell multi-omic analysis by profiling the entire genome and transcriptome simultaneously. In addition to single cell RNA sequencing, we can discuss how this method enables deep single cell genome sequencing, amplifying ultra-low quantities of DNA from individual cells. This facilitates the comprehensive detection of single nucleotide variants and chromosomal aberrations at single cell level. Let's talk 🙌 For more information: https://lnkd.in/eE_VkVq2 #SingleCellSequencing #NextGenSequencing #SingleCellTranscriptome #GenomeSequencing

Meghan Towne, MS, CGC, LGC, joined us from #NSGC23 to recap Poster GGT225: “Splicing Up the Diagnosis: Using Targeted RNA Studies to Reclassify Exome Sequencing Variants.” This analysis shows how targeted RNA studies can provide powerful evidence for VUS resolution. Learn more in this video. #genetictesting #RNA #VUS

Check out how RNA can be used for VUS resolution in exome analysis

🎉 Full-length RNA, single-cell RNA, and 16S rRNA sequencing to enable large-scale studies at a resolution difficult to attain with short-read RNA sequencing.

Want to learn more about FACS-based single-cell sequencing methods? I was recently a guest at the Single-Cell World podcast, where we talked about SORT-seq, tips&tricks during FACS analysis & the story behind SCD.

Is #ffpe #rna #sequencing challenging? Getting the best transcriptomics results out of your FFPE cohort requires expertise. GenomeScan offers you a comprehensive, robust, and reproducible solution for FFPE RNA analysis. FFPE, or formalin-fixed, paraffin-embedded, samples are tissues that have undergone the said methods for preservation. This method is commonly used for storing tissues in #biobanks for researching and diagnosing various diseases. Although a useful method, FFPE tissue storage can cause (partial) degradation of RNA, affecting the yield and sequencing. At GenomeScan, we provide you with a validated workflow including RNA #isolation from FFPE tissue blocks, RNA sequencing, and data analysis, that ensures reliability in your results. Visit our #rnaseq page for an overview of our service portfolio and learn more about how we work with FFPE samples. 👉 https://lnkd.in/ePgqEgd #genomescan #sequencing #ngs #biobank #biobanking #pathology #pathologie #oncology #oncologie #umc #transcriptomics

Why perform scRNA-seq? Here's a short snippet from our recent webinar on the origins and fundamentals of single cell RNA sequencing. Watch the full webinar here: https://lnkd.in/gSViNQur #singlecell #research

Thrilled to be able to share this Nature Communications paper I co-authored with Patricia T. detailing how dysfunction of an RNA binding protein (hnRNP A1) drives neurodegeneration in MS (check it out here: https://rdcu.be/dvqwA)!