{"database":"NODE","file_versions":[],"scores":null,"additional":{"omics_type":["Transcriptomics"],"submitter":["Yuanliang Zhang"],"technology_type":["ATAC-seq"],"full_dataset_link":["https://www.biosino.org/node/experiment/detail/OEX00027259"],"experiment_platform":["Illumina NovaSeq 6000"],"experiment_library_layout":["Paired"],"experiment_library_selection":["PCR"],"sample_count":["1"],"tissue":["['bone Marrow']"],"taxonomy":["['Mus musculus']"],"experiment_protocol":["A total of 1×105 BM LSKs from WT and KO-MDS mice were sorted, washed in DPBS, and lysed in 50 μL lysis buffer (10 mM Tris-HCl pH 7.4, 10 mM NaCl, 3 mM MgCl2, 0.1% (v/v) Igepal CA-630) for the follow-up process, which was performed by TruePrepTM DNA Library Prep Kit V2 for Illumina (TD501, Vazyme) according to the manufacturer’s instructions. Subsequently, the library fragments were purified by VAHTS DNA clean beads (Vazyme, N411-01) for future sequencing according to standard illumina HiSeq/NextSeq platform manuscripts."],"repository":["NODE"],"additional_accession":[]},"is_claimable":false,"name":"Old_LSK_ATAC_seq","description":"LSK (Lin-c-Kit+Sca1+) cells sorted from old Setd2 deficiency mice and control mice were used for ATAC sequencing.","dates":{"publication":"2024-02-27","submission":"2024-01-26"},"accession":"OEX00027259","cross_references":{"NODE":["OEP00004811"]}}