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We delivered these viruses in Ribotag mice using the PHP.eB serotype, either intracortically or systemically. We compared these samples with mice that received intracortical AAV2/5::GfaABC1D-Cre and transgenic Aldh1l1-CreERT2/Ribotag mice. We sequenced whole-tissue RNA as well as ribosomally-loaded astrocyte-enriched mRNA to assess cell-type specificity of viruses as well as virus-related transcriptomic changes. Overall design: Four cohorts were generated: Aldh1l1-CreERT2/Ribotag transgenic mice (control mice with highly astrocyte-specific labeled ribosomes) AAV2/5::GfaABC1D-Cre intracortical injection mice (standard astrocyte-enriched virus) PHP.eB::GfaABC1D-Cre-4x6T intracortical injection mice and PHP.eB::GfaABC1D-Cre-4x6T systemic injection mice. Each cohort included 4 mice, and each mouse had both input (whole-cortex) and immunoprecipitated (ribosomally loaded, astrocyte-enriched) mRNA samples.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Transcriptional analysis of murine cortical astrocytes with adeno-associated viral transduction with and without 4x6T miR cassette, vs transgenically labeled astrocytes</name><description>Transcriptional analysis of murine cortical astrocytes with adeno-associated viral transduction with and without 4x6T miR cassette, vs transgenically labeled astrocytes</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-03-06</first_public></dates><accession>PRJNA940089</accession><cross_references><GEO>GSE226366</GEO><taxon>10090</taxon><PubMed>37973910</PubMed></cross_references></HashMap>