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Characterization of Mechanotransduction-induced changes in cell identity of PDAC in response to Nanotopography - Session Live-seq & Biopsies
Pr. Dr. Carmelo FerraiDone
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Round Table - Live-seq & Biopsies
Done
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Single-cell Nanobiopsy Enables Multigenerational Longitudinal Transcriptomics of Cancer Cells - Session Live-seq & Biopsies
Dr. Fabio MarcuccioDone
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Welcome Note - FluidFM User Conference 2023
Done
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Pick and Place of Neuronal Cells and Spheroids using FluidFM for the Construction of Neuronal Networks - Session Mechanobiology
Dr. Sinead ConnollyDone
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Keynote Speaker - Robotic FluidFM in the Nanobiosensorics Lab: from large-area printing to high-throughput adhesion and injection of single cells - Session Mechanobiology
Dr. Robert HorvathDone
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Online - FluidFM – A versatile method in biomaterials research - Session Material Sciences
Dr. Christine Müller-RennoDone
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Social Activities in Zurich (*)
Done
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Coffee Break
Done
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Engineering Endosymbiotic Growth of E. coli in Mammalian Cells - Session Genome Engineering
Chantal ErnstDone
Deplancke Group, Laboratory of Systems Biology and Genetics.
EPFL. Lausanne, Switzerland
For Dr. Orane Guillaume-Gentil' FluidFM success story:
More information available here.
Abstract: In this talk, I will share my research on Live-seq, a transformative single-cell transcriptomics approach that does not require cell isolation and lysis. Live-seq uses FluidFM Nanosyringes to retrieve cytosolic picoliter biopsies from living cells, which are then analyzed with a highly-sensitive, ultra-low input RNA-seq protocol. The resulting gene expression profiles are faithful representations of intact cell transcriptomes, while the sampled cells remain alive and functional in their original microenvironment. Live-seq makes it therefore possible to perform spatially-resolved longitudinal profiling and phenotyping of individual cells, unlocking exciting opportunities for investigating cellular dynamics and cell-cell communication.
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