{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR323/093/SRR32358993/SRR32358993.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR323/092/SRR32358992/SRR32358992.fastq.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["Southern Medical University"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA1224241"],"long_description":["ATAC-seq pipeline was utilized for stringent quality control and statistical analysis of sequencing data, ensuring the reliability of accessibility profiles. Paired-end reads (150 bp) were aligned to the reference genome (human: hg38 mouse: mm10) following a standardized mapping protocol. To detect differentially accessible regions, the DiffBind R package was employed, using statistical modeling to identify significant chromatin accessibility variations between conditions."],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"","description":"ATAC-sequence in H69AR and H69 celllines","dates":{"last_updated":"2025-02-22","first_public":"2025-02-22"},"accession":"PRJNA1224241","cross_references":{}}