PicoPLEX single-cell DNA-seq: detection of CNV and SNV from single cells
Accurate, reproducible detection of single nucleotide variation (SNV) and copy number variation (CNV) from small amounts of DNA, single cells, or fixed tissue is critical for genetic analysis of clinical samples, with the broader goal of assisting the molecular diagnosis of diseases such as cancer. In this webinar, Dr. Luke Sherlin showcases our optimized PicoPLEX technology—the PicoPLEX Gold Single Cell DNA-Seq Kit (PicoPLEX Gold)—a rapid and easy-to-use system for generating DNA-seq libraries from as little as 1–10 cells for the highly sensitive detection of SNV, CNV, or other genomic aberrations.
Key features of PicoPLEX Gold covered in the webinar:
- Fast, simple workflow—from cells to libraries in 3 hr, with minimal hands-on time
- Best-in-class performance—superior coverage, complexity, and sensitivity compared to MDA
- Flexible kit configuration—choose from a variety of different indexing options for any experiment and Illumina sequencer
About the presenter
Luke Sherlin, PhD
Luke Sherlin was previously a Product Manager for Takara Bio USA's NGS portfolio. He has been in the biotech industry for 12+ years, with positions in technical support and marketing. He holds a PhD degree in Chemistry from the University of California, Santa Barbara.
Takara Bio USA, Inc.
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