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资源简介：
genome editing statistics_deep sequence
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创建时间：
2023-02-07
相关数据集
FnCas12a-mediated Eimeria tenenlla genome knock out
Detected edit efficiency of FnCas12a
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CRISPRscan: designing highly efficient sgRNAs for CRISPR-Cas9 targeting in vivo. Danio rerio
Variable activity across different single guide RNAs (sgRNAs) remains a significant limitation of the CRISPR/Cas9 system. We have identified molecular features that influence sgRNA stability, activity
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Additional file 2 of Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids
Additional file 2: Table S1. Individual data values of all data represented in this manuscript.
Figshare2023-07-14 更新30
Phosphonoacetate Modifications Enhance the Stability and Editing Yields of Guide RNAs for Cas9 Editors
CRISPR gene editing and control systems continue to emerge and inspire novel research and clinical applications. Advances in CRISPR performance such as optimizing the duration of activity in cells, ti
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Homo sapiens and zebrafish Targeted Locus (Loci)
We find that pre-crRNAs comprising a full-length direct repeat (full-DR-crRNA) sequence with specific stem-loop G-C base substitutions exhibit increased editing efficiencies compared with the standard
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