Abstract
DeRisi and colleagues present a creative application for Cas9 in vitro, using it to deplete unwanted sequence from DNA libraries. It seems plausible that the in vitro use of CRISPR/Cas9 has unrealized potential to revolutionize the practice of molecular biology well beyond genome editing.
MeSH terms
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CRISPR-Cas Systems / genetics
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Communicable Diseases / genetics
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High-Throughput Nucleotide Sequencing / methods*
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Humans
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Neoplasms / genetics
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Nucleic Acid Hybridization / methods*
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RNA / genetics
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RNA Editing / genetics
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RNA, Mitochondrial
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RNA, Ribosomal / genetics
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Sequence Analysis, DNA*
Substances
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RNA, Mitochondrial
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RNA, Ribosomal
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RNA