Detection of CNVs and SNVs from single cells to decipher molecular mechanisms of diseases

Accurate, reproducible detection of genomic variants such as single nucleotide variants (SNVs) and copy number variants (CNVs) 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.

Join our webinar and learn how to achieve SNV and CNV detection from single cells with the highest sensitive and reproducible single-cell NGS technology SMARTer PicoPLEX Gold Single Cell DNA-Seq (PicoPLEX Gold). Our European NGS Product Manager, Matthieu Pesant, presents:

  • The PicoPLEX Gold streamlined workflow for single cell whole-genome amplification library preparation
  • How CNVs and SNVs can be efficiently and reproducibly detected in single cells
  • Data generated by Takara Bio demonstrating the use of PicoPLEX Gold with amplicon-based enrichment for fast and accurate SNV and CNV detection with shallow sequencing
Matthieu Pesant, PhD


Matthieu Pesant, PhD
European NGS Product Manager
Takara Bio Europe