<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Marek Bartkuhn</submitter><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16258</full_dataset_link><description>Pregnant wild type C57BL/6J mice were randomized at 15.5 dpc or 18.5 dpc to receive intraperitoneal (i.p.) injection of saline, LPS 50 μg/kg (LPS 50) or LPS 100 μg/kg (LPS 100). At birth, newborn pups were euthanized and 2 lobes of the right lung were removed and frozen in liquid nitrogen for RNA extraction. A total amount of 500 ng of RNA per sample was used to enrich for polyadenylated mRNA followed by sequencing.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - cDNA libraries were sequenced on the Illumina NovaSeq 6000 platform generating 50 bp paired-end reads.</sample_protocol><sample_protocol>Sample Collection - Cranial and accessory lobes of the right lung were removed and frozen in liquid nitrogen</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was extracted using the RNeasy Mini Kit automatically via QIAcube®Connect (Qiagen, Hamburg, Germany).</sample_protocol><sample_protocol>Library Construction - 500 ng of RNA per sample was used to enrich for polyadenylated mRNA followed by cDNA sequencing library preparation utilizing the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina®.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Demutliplexing and FASTQ extraction was performed using bcl2fastq v2.20.0.422. Primary processing of FASTQ data including quality control, filtering, trimming,alignment of reads and counting of gene-sprecific genes was done using nf-core RNA-seq pipeline v3.7 Processed data files contain raw sequencing counts per gene as determined by nf-core rna-seq pipeline.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Mus musculus</species><pubmed_authors>Ying Dong</pubmed_authors><pubmed_authors>Marek Bartkuhn</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prenatal LPS infection impacting on neonatal mice lung at birth</name><description>Pregnant wild type C57BL/6J mice were randomized at 15.5 dpc or 18.5 dpc to receive intraperitoneal (i.p.) injection of saline, LPS 50 μg/kg (LPS 50) or LPS 100 μg/kg (LPS 100). At birth, newborn pups were euthanized and 2 lobes of the right lung were removed and frozen in liquid nitrogen for RNA extraction. A total amount of 500 ng of RNA per sample was used to enrich for polyadenylated mRNA followed by sequencing.</description><dates><release>2026-01-08T00:00:00Z</release><modification>2026-01-08T19:53:11.311Z</modification><creation>2025-11-21T16:38:20.693Z</creation></dates><accession>E-MTAB-16258</accession><cross_references><ENA>ERP185492</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>