ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/009/SRR30230409/SRR30230409_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/008/SRR30230408/SRR30230408_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/006/SRR30230406/SRR30230406_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/005/SRR30230405/SRR30230405_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/009/SRR30230409/SRR30230409_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/006/SRR30230406/SRR30230406_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/007/SRR30230407/SRR30230407_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/010/SRR30230410/SRR30230410_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/010/SRR30230410/SRR30230410_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/005/SRR30230405/SRR30230405_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/008/SRR30230408/SRR30230408_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR302/007/SRR30230407/SRR30230407_1.fastq.gzprimaryOK200GenomicsGhent Universityhttps://www.ebi.ac.uk/ena/browser/view/PRJNA1147920xref:EuropePMC:PMC11834386Nezara viridula adult females were injected with the SYNCAS CRISPR-Cas9 formulation targeting the orthologue of Drosophila melanogaster white. DNA was extracted from resulting offspring and a PCR was performed amplifying the target region. PCR product was then used for amplicon sequencing to analyze mutations in the DNA pool.ENAfalseNezara white gene CRISPR-Cas9 editing2025-01-312025-01-31PRJNA1147920