<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/GSE305nnn/GSE305673/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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><gds_type> Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE305673</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Dysregulated differentiation kinetics underlie essential role of DNA damage repair in cloned placentas [scMutiomics]</name><description>To investigate the mechanisms underlying cloned placenta hyperplasia, we employed single-nuclei RNA and ATAC-seq multi-omics at the critical window of placental overgrowth. Our work offers the first comprehensive and novel single-nuclei–level dissection of developmental barriers in SCNT placentas, demonstrating that genomic instability constitutes the principal determinant of SCNT placental dysfunction, and outlines a feasible approach to improve reproductive cloning outcomes.</description><dates><publication>2026/06/18</publication></dates><accession>GSE305673</accession><cross_references><GSM>GSM9675360</GSM><GSM>GSM9675362</GSM><GSM>GSM9675361</GSM><GSM>GSM9181681</GSM><GSM>GSM9181680</GSM><GSM>GSM9181683</GSM><GSM>GSM9675359</GSM><GSM>GSM9181682</GSM><GSM>GSM9181678</GSM><GSM>GSM9181677</GSM><GSM>GSM9181679</GSM><GSM>GSM9181685</GSM><GSM>GSM9181674</GSM><GSM>GSM9181673</GSM><GSM>GSM9181684</GSM><GSM>GSM9181676</GSM><GSM>GSM9181686</GSM><GSM>GSM9181675</GSM><GPL>34290</GPL><GSE>305673</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>