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poster

Subclonal identification of driver mutations and copy number variations from single-cell DNA sequencing of tumors


James Flynn, PhD
ABRF (2020)

Single-cell sequencing elucidates unique insights in understanding intratumor heterogeneity and clonal evolution. Both chromosomal structural change/copy number alteration/variation (CNA/CNV) and driver gene mutation events appear somatically at the early stages of oncogenesis and are critical in cancer initiation, tumor progression, and therapy response. We have developed a high-throughput single-cell DNA analysis platform that leverages droplet microfluidics and a multiplex-PCR-based targeted DNA sequencing approach. The platform demonstrates high-sensitivity detection of SNVs and indels in the same cells and generation of high-resolution maps of clonal architecture based on mutational profiling.


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Manimozhi Manivannan
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Powerful insights with single-cell multi-omics: Co-detecting both genotype and phenotype from the same cell
James Flynn, PhD
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Single-cell multi-omics for simultaneous detection of SNVs, CNVs, and proteins using the Tapestri Platform
Aik Ooi, PhD
AMP (2019)
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