Genome sequencing of CRISPR-Cas9 nickase generated clpP1 and clpP2 mutants in Clostridioides difficile strain 630
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资源简介：
We used a CRISPR-Cas9 nickase genetic editing system to insert stop codons into the clpP1 and clpP2 genes in Clostridioides difficile strain 630. The genomes of each mutant were re-sequenced to confirm the absence of any off targets.
创建时间：
2020-11-06
