CRISPR-Cas13 allows selective modification of desired RNA in living cells
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Researchers have developed a new tool using CRISPR-Cas13 that allows for the selective modification of desired RNA in living cells. This technology enables precise chemical modification of RNA and may have applications in identifying multiple viruses and variants simultaneously. The CRISPR-Cas13 system also appears to offer various modes of control, including on and off gene regulation and targeted chemical modification of specific RNA.
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