<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/GSE334nnn/GSE334068/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE334068</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Integrative transcriptomic profiling of pediatric bone marrow failure syndromes: shared coding and long non-coding RNA signatures</name><description>Pediatric bone marrow failure (BMF) comprises inherited and immune-mediated disorders, many of which remain genetically unclassified. We performed total RNA sequencing of bone-marrow aspirates from pediatric BMF patients and controls to identify shared coding and long non-coding RNA (lncRNA) transcriptional signatures across genetically-defined (g-BMF) and genetically-undefined (u-BMF) disease. This record provides processed gene-level quantification (raw counts and CPM) for all 14 samples; raw sequencing reads are in SRA under BioProject PRJNA1406476.</description><dates><publication>2026/08/12</publication></dates><accession>GSE334068</accession><cross_references><GSM>GSM9779890</GSM><GSM>GSM9779891</GSM><GSM>GSM9779900</GSM><GSM>GSM9779889</GSM><GSM>GSM9779901</GSM><GSM>GSM9779902</GSM><GSM>GSM9779892</GSM><GSM>GSM9779893</GSM><GSM>GSM9779894</GSM><GSM>GSM9779895</GSM><GSM>GSM9779896</GSM><GSM>GSM9779897</GSM><GSM>GSM9779898</GSM><GSM>GSM9779899</GSM><GPL>24676</GPL><GSE>334068</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>