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Precise and Predictable CRISPR Chromosomal Rearrangement Editing Reveals Principles of Cas9-mediated Nucleotide Insertion

NIAID Data Ecosystem2026-03-10 收录

CRISPRi基因编辑

Cas9介导核苷酸插入

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA454744 数据链接链接失效反馈

官方服务：

资源简介：

DNA fragment editing by CRISPR/Cas9

应用场景：

创建时间：

2018-05-02

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CRISPR edited strains generated.

CRISPRi基因编辑

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S6 Table lists information regarding alleles, strain names and reagents that were generated and used, respectively, during this study for CRISPR/Cas9 mediated genome engineering. (XLSX)

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CRISPR RNA-seq from HepG2 (ENCSR994NGU)

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RNA-seq on HepG2 cells treated with a CRISPR gRNA against RPS8. (RPS8-BGHcLV31) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Res

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File S2.zip

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基因敲入序列分析

Annotated sequence files in .ape format (comparable with Genbank) of knock-ins generated by CRISPR/Cas9-mediated genome editing. Unmodified genomic sequence is also provided.

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The uncropped raw gel images.xlsx

CRISPRi基因编辑

凝胶电泳验证

Herein, we present the uncropped raw gel images associated with our manuscript titled " Enhancement of CRISPR-Cas12a System through Universal Circular RNA Design ," published in Cell Reports M

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AlleleAnalyzer supporting data

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The CRISPR/Cas system is a highly specific genome editing tool capable of distinguishing alleles differing by even a single base pair. Target sites might carry genetic variations that are not distin

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