Sequencing of a pooled CRISPR/Cas library for N. oceanica
收藏NIAID Data Ecosystem2026-05-02 收录
官方服务：
资源简介：
Sequencing the gRNA library, plasmid library, mutants and FlowRACS-sorted libraries.
应用场景：
创建时间：
2025-07-02
相关数据集
Expanding the Potential of CRISPR-Cpf1-Based Genome Editing Technology in the Cyanobacterium Anabaena PCC 7120
CRISPR systems, such as CRISPR-Cas9 and CRISPR-Cpf1, have been successfully used for genome editing in a variety of organisms. Although the technique of CRISPR-Cpf1 has been applied in cyanobacteria r
NIAID Data Ecosystem80
CRISPR library targeting lncRNA and protein coding genes along BLaER1 transdifferentiation (Replicate 2)
CRISPR library screening experiment in BLaER-Cas9 cells that were induced to transdifferentiate into macrophages. The purpose of the experiment is to discover novel players (lncRNAs and protein-coding
NIAID Data Ecosystem40
Chlamydomonas reinhardtii synthetic chromosomes and centromeres
Quoted from NSF Award Abstract #2151106Some of the most pressing problems in agriculture and biotechnology can only be tackled by large scale changes in crop or host genomes where multiple genes must
NIAID Data Ecosystem20
Evaluation of off-target effects of the Cas9 in a knock-out Phaeodactylum tricornutum strain. Phaeodactylum tricornutum strain:Pt1
We used the combination of CRISPR/Cas9 and bacterial conjugation to edit thePhatr3_J46193 gene in the P. tricornutum genome. Since there are no reports of the occurrence of off-target changes at the g
NIAID Data Ecosystem80
Pt4 Lhcx1 knockout using TALEN. Phaeodactylum tricornutum (strain4) knockouts
We generated knockout lines of the antenna protein Lhcx1 in Phaeodactylum tricornutum using a TALEN approach. We designed two TALEN pairs and greated three knockout lines (x1KO_1a/1b and x1KO_2)
NIAID Data Ecosystem30
