American Society of Human Genetics
Discover more biomarkers with Shasta NGS technologies
The 2024 ASHG Annual Meeting, happening November 5–9 in Denver, CO, brings together scientists and patient care professionals from academia, industry, government and the non-profit sectors to learn about the newest research and technology in the fields of human genetics and genomics. Join us for an industry education session featuring two scientists who will discuss their research using our brand new Shasta Single Cell System or visit us at booth 877 to view our featured posters. We will share our complete, novel solutions that can drive biomarker discovery and help you develop pioneering single-cell NGS assays using more cells than ever before.
Industry education session
November 6 at 3:00 pm in Room 102
Refining acute leukemia genomics through single-cell sequencing
In this talk, Dr. Ilaria Iacobucci from St. Jude Children's Research Hospital speaks about using single-cell sequencing of acute leukemia samples to dissect clonal diversity at an unprecedented resolution. This provides insights into the dynamic process of clonal evolution and allows for a more accurate understanding of disease pathogenesis and classification.
TE-chimeric transcripts in cancer: From bulk to single-cell
In this talk, Colin McCornack from the Wang Lab at Washington University in St. Louis speaks about their recent work on the co-opting of transposable elements as cis-regulatory elements in cancer, with a special emphasis on recent efforts to uncover expression at the single-cell level using the new Shasta Single Cell System.
Featured posters
November 5–9 at the Takara Bio booth
A novel, high-throughput, full gene-body scRNA-seq workflow for improved biomarker discovery
With this poster, we present how the Shasta Single Cell System enables the preparation of high-quality, full-gene body RNA-seq libraries for up to 100,000 single cells per run with a unique barcoding strategy, which significantly improves the identification of new biomarkers.
Resolving tumor heterogeneity with a fully automated, high-throughput single-cell WGA workflow
With this poster, we present how Shasta technology increases the cell throughput of single-cell WGA from 96 to 1,500 cells per run and enables the reliable detection of CNVs and SNVs at a shallow sequencing depth.
More cells. More biomarkers. More discoveries.
Want to go from sample prep through data analysis with less hands-on time and stress? Meet the Shasta Single Cell System, which helps oncology researchers find novel biomarkers. Learn how our high-throughput Shasta technologies can inspire the next breakthrough.
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