Accounting for diversity in the design of CRISPR-based therapeutic genome editing.

Accounting for diversity in the design of CRISPR-based therapeutic genome editing.
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考虑基于CRISPR的治疗基因组编辑设计的多样性。

DOI:
10.1038/s41588-022-01272-z
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发表时间:
2023-01
期刊:
影响因子:
30.8
通讯作者:
Saha K
Saha K
中科院分区:
生物学1区
文献类型:
--
作者:
Saha K

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CRISPR细胞/基因疗法的设计主要基于单一参考人类基因组。一项新的研究揭示了人类遗传多样性如何导致脱靶效应,并提出了一种识别这些风险的新工具。
CRISPR cell/gene therapy has been designed largely based on a single reference human genome. A new study reveals how human genetic diversity could lead to off-target effects and presents a novel tool to identify these risks.
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