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CRISPR/Cas9-engineered cancer models: the next step forward for targeted cancer therapy

The advent of CRISPR/Cas9 gene editing, together with the plummeting cost of whole-genome sequencing, has cleared a path for the development of customised cancer cell models. Here, we discuss recent developments in the field and challenges associated with targeted-therapy resistance.











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This content is provided to you for free thanks to the kind support of our sponsors: Agilent, BMG Labtech, ForteBio, Sartorius

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