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- W2892376729 abstract "Existing methods to enrich target regions of genomic DNA based on PCR, hybridization capture, or molecular inversion probes have various drawbacks, including long experiment times and low throughput and/or enrichment quality. We developed CRISPR-Cap, a simple and scalable CRISPR-based method to enrich target regions of dsDNA, requiring only two short experimental procedures that can be completed within two hours. We used CRISPR-Cap to enrich 10 target genes 355.7-fold on average from Escherichia coli genomic DNA with a maximum on-target ratio of 81% and high enrichment uniformity. We also used CRISPR-Cap to measure gene copy numbers and detect rare alleles with frequencies as low as 1%. Finally, we enriched coding sequence regions of 20 genes from the human genome. We envision that CRISPR-Cap can be used as an alternative to other widely used target-enrichment methods, which will broaden the scope of CRISPR applications to the field of target enrichment field." @default.
- W2892376729 created "2018-09-27" @default.
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- W2892376729 date "2018-09-12" @default.
- W2892376729 modified "2023-10-07" @default.
- W2892376729 title "CRISPR-Cap: multiplexed double-stranded DNA enrichment based on the CRISPR system" @default.
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- W2892376729 doi "https://doi.org/10.1093/nar/gky820" @default.
- W2892376729 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6326800" @default.
- W2892376729 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30215766" @default.
- W2892376729 hasPublicationYear "2018" @default.
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