Genome-wide CRISPR knockout library screening coupled with high-throughput sequencing to analyze DNA repair outcomes
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ABSTRACT: Cells were transduced with a genome-wide CRISPR knockout library to introduce gene disruptions across the genome. After Cas9-induced DNA double-strand breaks, repair outcomes were captured and quantified using high-throughput sequencing. This experiment aims to identify genetic factors influencing specific DNA repair outcome patterns such as 1-bp insertions, microhomology-mediated deletions, and large insertions.
INSTRUMENT(S): Illumina NovaSeq 6000
ORGANISM(S): Homo sapiens
SUBMITTER: Yanbin Wan
PROVIDER: E-MTAB-15874 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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