<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/GSE300nnn/GSE300655/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE300655</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Expression data of E13.5 placenta from intra-cytoplasmic sperm injection(ICSI)-F2 offspring</name><description>Various behavioural abnormalities and congenital anomalies were observed in the F2 offspring of ICSI (Kanatsu-Shinohara et al., 2023, J. Clin.). Invest. 133(22): e170140). The data presented here aim to clarify the cause of these abnormalities. Gene expression in the ICSI-F2 placenta was investigated using RNA sequencing (RNA-seq). ICSI was performed using C57BL/6 epididymal sperm and oocytes. Male ICSI-F2 offspring was mated with wild-type C57BL/6 female, and placentae recovered from pregnant females at E13.5 were examined for gene expression. Each group contains five biological replicates.</description><dates><publication>2026/04/21</publication></dates><accession>GSE300655</accession><cross_references><GSM>GSM9065878</GSM><GSM>GSM9065879</GSM><GSM>GSM9065876</GSM><GSM>GSM9065877</GSM><GSM>GSM9065875</GSM><GSM>GSM9065883</GSM><GSM>GSM9065884</GSM><GSM>GSM9065881</GSM><GSM>GSM9065882</GSM><GSM>GSM9065880</GSM><GPL>13112</GPL><GSE>300655</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>