<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/SRR687/000/SRR6876050/SRR6876050_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/001/SRR6876051/SRR6876051_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/008/SRR6876048/SRR6876048_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/001/SRR6876051/SRR6876051_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/000/SRR6876050/SRR6876050_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/009/SRR6876049/SRR6876049_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/009/SRR6876049/SRR6876049_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR687/008/SRR6876048/SRR6876048_1.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>Bioinformatics Core Facility, Wellcome Centre for Cell Biology, University of Edinburgh</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA442754</full_dataset_link><scientific_name>Saccharomyces cerevisiae</scientific_name><tag>xref:PubMed:31031198</tag><long_description>ChIP-seq profile of Spo13 binding sites arrested in prophase I by deletion of the meiotic transcription factor NDT80. Previous ChIP-ChIP data had indicated that Spo13 binding correlates with cohesin binding sites. Therefore, in addition to wild type cells, we also investigated cells deficient of the meiosis-specific cohesin subunit Rec8 to identify cohesin-dependent binding sites of Spo13. Overall design: Diploid S. cerevisiae SK1 cells were constructed containing Spo13-3Flag in an ndt80Δ background. Cells were allowed to sporulate in sporulation media for 5 hours after which formaldehyde was added to the cultures and cells were fixed for 30min. Samples were then processed according to the standard lab ChIP-Seq protocol.</long_description><repository>ENA</repository><description_synonyms>SPNGAF60, meiosis I nuclear division, wide, count in organism, absence, absent from organism., wide/broad, Genomes, ligand, number, whole genome, broad, presence</description_synonyms><name_synonyms>SPNGAF60, meiosis I nuclear division, wide, count in organism, absence, absent from organism., wide/broad, Genomes, ligand, number, whole genome, broad, presence</name_synonyms></additional><is_claimable>false</is_claimable><name>Genome-wide binding of the meiosis I-specific Spo13 in the presence and absence of cohesin</name><description>Genome-wide binding of the meiosis I-specific Spo13 in the presence and absence of cohesin</description><dates><last_updated>2025-09-24</last_updated><first_public>2019-04-26</first_public></dates><accession>PRJNA442754</accession><cross_references><GEO>GSE112170</GEO><taxon>4932</taxon><PubMed>31031198</PubMed></cross_references></HashMap>