<HashMap><database>NODE</database><scores/><additional><omics_type>Transcriptomics</omics_type><submitter>Yuanliang Zhang</submitter><technology_type>RNA-Seq</technology_type><full_dataset_link>https://www.biosino.org/node/experiment/detail/OEX00027260</full_dataset_link><experiment_platform>Illumina NovaSeq 6000</experiment_platform><experiment_library_layout>Paired</experiment_library_layout><experiment_library_selection>PCR</experiment_library_selection><sample_count>1</sample_count><tissue>['bone Marrow, Liver']</tissue><taxonomy>['Mus musculus']</taxonomy><experiment_protocol>For bulk RNA-seq, total RNA samples were extracted, and ribosomal RNA (rRNA) was removed using the Ribo-Zero rRNA Removal Kit (MRZMB126, Illumina). Subsequently, rRNA-depleted samples were fragmented, then subjected to first and second strand cDNA synthetization. cDNAs were ligated with sequencing adapters according to standard Novaseq 6000 platform (Illumina) manuscripts.</experiment_protocol><repository>NODE</repository></additional><is_claimable>false</is_claimable><name>Old_RNA-seq</name><description>cells from WT and Setd2 deficiency mice were sorted for RNA sequencing.</description><dates><publication>2024-02-27</publication><submission>2024-01-26</submission></dates><accession>OEX00027260</accession><cross_references><NODE>OEP00004811</NODE></cross_references></HashMap>