Bulk-ATAC sequencing in RUNX-altered murine lung adenocarcinoma cell lines

ABSTRACT: Here, we using CRISPR activation and knockout studies to assess the implication of dysregulation of RUNX transcription factors on chromatin accessibility using bulk ATAC-sequencing. Tumor cell lines were derived from primary Kras G12D; p53 mutant mice (KP model) after initiation of tumors with SPC-Cre, resulting in lung adenocarcinoma. Cell lines were then expanded and profiled using bulk ATAC-sequencing.

ORGANISM(S): Mus musculus

PROVIDER: GSE151403 | GEO | 2020/07/23

REPOSITORIES: GEO