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The genome-wide binding sites of transcription factors provide insight into their regulatory function. We used chromatin immunoprecipitaition with high-throughput sequencing (ChIP-seq) to identify the genomic binding sites of HNF4A and GATA6 in OE19 cells.
ORGANISM(S): Homo sapiens 
Open chromatin profiling (ATAC-seq) of human oesophageal adenocarcinoma patient samples.
ORGANISM(S): Homo sapiens 
To identify DNA binding sites of KLF5 in CP-A and OE19 cells, we carried out ChIP-seq.
ORGANISM(S): Homo sapiens 
The open chromatin of Barrett's oesophagus cell line CP-A has been profiled by ATAC-seq.
ORGANISM(S): Homo sapiens 
Barrett's esophagus is the assumed precusor to oesophageal adenocarcinoma. We profiled the open chromatin of human Barrett's biopsies to gain insight into its molecular basis.
ORGANISM(S): Homo sapiens 
To identify active regulatory regions of the genome, we performed H3K27ac ChIP-seq.
ORGANISM(S): Mus musculus 
To determine the ability of HNF4A and GATA6 to drive open chromatin formation, either HNF4A or GATA6 were overexpressed in normal oesophageal Het1A cells and ATAC-seq was performed.
ORGANISM(S): Homo sapiens 
The open chromatin of new esophageal adenocarcinoma cell line MFD-1 has been profiled by ATAC-seq.
ORGANISM(S): Homo sapiens 
To investigate the role of transcription factors in oesophageal adenocarcinoma, transcription factors were knocked down using siRNA and RNA was extracted and sequenced to identify target genes.
ORGANISM(S): Homo sapiens 
To identify the transcriptional targets of Foxa2, we treated Fh1-WT or Fh1-KO cells with either siNT or siFoxa2 and subsequent RNA-sequencing.
ORGANISM(S): Mus musculus 
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