<HashMap><database>NODE</database><scores/><additional><omics_type>Transcriptomics</omics_type><submitter>Jiayin Peng</submitter><technology_type>RNA-Seq</technology_type><full_dataset_link>https://www.biosino.org/node/experiment/detail/OEX00021151</full_dataset_link><experiment_platform>Illumina HiSeq 1500</experiment_platform><experiment_library_layout>Paired</experiment_library_layout><experiment_library_selection>size fractionation</experiment_library_selection><experiment_mate_pair>N</experiment_mate_pair><sample_count>1</sample_count><tissue>['skeletal Muscle']</tissue><taxonomy>['Mus musculus']</taxonomy><experiment_protocol>For Gli1+MuSCs, a total of 8,508 tdT+ (Gli1+) cells were sorted from hindlimb skeletal muscles of 3 adult male mice and pooled for scRNA-seq.

  For WT MuSCs,  CD45-CD31-Sca1-Vcam1+ MuSCs were isolated from wild-type mice by fluorescence-activated cell sorting (FACS),and analyzed by scRNA-seq.</experiment_protocol><repository>NODE</repository></additional><is_claimable>false</is_claimable><name>OEX_Jiayin_2212211338</name><description>We performed scRNA-seq using Gli1-CreERT2; R26-tdTomato mice, in which Gli1+ cells were labeled by tdTomato (tdT) after tamoxifen (TAM) induction. 

  CD45-CD31-Sca1-Vcam1+ MuSCs were isolated from wild-type mice by fluorescence-activated cell sorting (FACS),and analyzed by scRNA-seq.</description><dates><publication>2023-08-01</publication><submission>2022-12-21</submission></dates><accession>OEX00021151</accession><cross_references><NODE>OEP00003799</NODE></cross_references></HashMap>