{"database":"NODE","file_versions":[],"scores":null,"additional":{"omics_type":["Transcriptomics"],"submitter":["Jiayin Peng"],"technology_type":["RNA-Seq"],"full_dataset_link":["https://www.biosino.org/node/experiment/detail/OEX00021151"],"experiment_platform":["Illumina HiSeq 1500"],"experiment_library_layout":["Paired"],"experiment_library_selection":["size fractionation"],"experiment_mate_pair":["N"],"sample_count":["1"],"tissue":["['skeletal Muscle']"],"taxonomy":["['Mus musculus']"],"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.\n\n  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."],"repository":["NODE"],"additional_accession":[]},"is_claimable":false,"name":"OEX_Jiayin_2212211338","description":"We performed scRNA-seq using Gli1-CreERT2; R26-tdTomato mice, in which Gli1+ cells were labeled by tdTomato (tdT) after tamoxifen (TAM) induction. \n\n  CD45-CD31-Sca1-Vcam1+ MuSCs were isolated from wild-type mice by fluorescence-activated cell sorting (FACS),and analyzed by scRNA-seq.","dates":{"publication":"2023-08-01","submission":"2022-12-21"},"accession":"OEX00021151","cross_references":{"NODE":["OEP00003799"]}}