<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE249nnn/GSE249551/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE249551</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell muti-omics delineates the dynamics of distinct epigenetic codes coordinating mouse gastrulation</name><description>Our study used CoBATCH to profile the H3K27ac and H3K4me1 states in mouse embryos at six continuous developmental stages ranging from Pre-Primitive Streak to Early Headfold stages, we comprehensively analyzed two histone markers and integrative scRNA-seq query dataset. Finally, we constructed a gene regulatory network centered on pivotal transcription factors and unraveled the mechanisms of how enhancers usage coordinates the transition of gene expression along lineage progression.</description><dates><publication>2024/10/01</publication></dates><accession>GSE249551</accession><cross_references><GSM>GSM7949971</GSM><GSM>GSM7949970</GSM><GSM>GSM7949964</GSM><GSM>GSM7949963</GSM><GSM>GSM7949974</GSM><GSM>GSM7949973</GSM><GSM>GSM7949972</GSM><GSM>GSM7949968</GSM><GSM>GSM7949967</GSM><GSM>GSM7949966</GSM><GSM>GSM7949965</GSM><GSM>GSM7949969</GSM><GPL>24247</GPL><GSE>249551</GSE><taxon>Mus musculus</taxon><PMID>[40340740]</PMID></cross_references></HashMap>