EMX1 gene editing sequencing

NIAID Data Ecosystem2026-05-01 收录

CRISPRi基因编辑

基因编辑效率评估

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1096627 数据链接链接失效反馈

官方服务：

资源简介：

The goal is to assess the efficiency of gene editing using CRISPR-Cas9.

创建时间：

2024-04-05

CRISPR RNA-seq from K562 (ENCSR234FWR)

CRISPRi基因编辑

转录组分析

RNA-seq on K562 cells treated with a CRISPR gRNA against RPL28. (RPL28-BGKcLV15) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Re

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File S2.zip

CRISPRi基因编辑

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.

Figshare2023-03-14 更新20

CRISPR RNA-seq from K562 (ENCSR929YET)

CRISPRi基因编辑

转录组分析

RNA-seq on K562 cells treated with a CRISPR gRNA against AIMP1. (AIMP1-BGKcLV26) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Re

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CRISPR RNA-seq from HepG2 (ENCSR194SPW)

CRISPRi基因编辑

肝癌基因表达

Control CRISPR gRNA against no target in HepG2 cells followed by RNA-seq. (NT-BGHcLV07-B) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov

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Frequency of INDEL formation in mice using gRNA synthesized from pU6T7 expression vectors.

CRISPRi基因编辑

INDEL突变频率

Frequency of INDEL formation in mice using gRNA synthesized from pU6T7 expression vectors.

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