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SMARTer 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 molecular diagnosis of diseases such as cancer. In this webinar, Dr. Luke Sherlin showcases our optimized PicoPLEX technology—the SMARTer 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 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
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