<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR323/093/SRR32358993/SRR32358993.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR323/092/SRR32358992/SRR32358992.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Southern Medical University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1224241</full_dataset_link><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.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name></name><description>ATAC-sequence in H69AR and H69 celllines</description><dates><last_updated>2025-02-22</last_updated><first_public>2025-02-22</first_public></dates><accession>PRJNA1224241</accession><cross_references/></HashMap>