Abstract:Ever since its discovery, CRISPR-Cas9 has taken over the world in gene editing. By providing a single guide RNA to the cas9 enzyme, CRISPR-Cas9 can immediately pinpoint the target gene location in the genome and slice it. Scientists discovered a revolutionary way to use this method for gene editing. Yet, the challenge is that the CRISPR-Cas9 system is lenient with the matching precision of the guide RNA to the target sequence As a result, the CRISPR-cas9 system may also cleave certain healthy sequences that ar… Show more
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