<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/GSE346nnn/GSE346710/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE346710</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Allele-resolved liver transcriptomes of CC032 x CC072 F1 mice quantified against a Collaborative Cross founder pantranscriptome</name><description>RNA-seq on liver tissue from the same two 25-day-old CC032 x CC072 F1 hybrid mice profiled by ATAC-seq in GSE345488 (F19 and F20). Reads were aligned to a spliced Collaborative Cross founder pangenome, which represents each Ensembl transcript by the distinct sequences it takes across the founders, and quantified in a haplotype-aware manner: at each gene the most likely founder-haplotype pair is inferred from read compatibilities, and abundance is then estimated for each haplotype-specific transcript of that pair. The data accompany the allele-specific chromatin accessibility analysis and allow accessibility and expression to be compared haplotype by haplotype in the same animals.</description><dates><publication>2026/09/16</publication></dates><accession>GSE346710</accession><cross_references><GSM>GSM10038966</GSM><GSM>GSM10038967</GSM><GPL>24247</GPL><GSE>346710</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>