<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR145/092/SRR14574892/SRR14574892.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR145/093/SRR14574893/SRR14574893.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Soochow University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA730705</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>We report the application of RNA sequencing technology for high-throughput profiling of gene expression in mammalian cells. By sequencing from mouse embryonic fibroblasts RNA, we generated genome-wide gene expression maps of mouse embryonic fibroblasts cells. We found a significant difference of relatived gene in Ahi1+/+and Ahi1-/- cells in the basal state. These findings help to understand more functions and roles of the Ahi1 gene. Overall design: Mouse embryonic fibroblasts cell mRNA profiles of wild type (WT) and Ahi1-/- mice</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and Ahi1-/- mouse embryonic fibroblasts cells Transcriptomes</name><description>Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and Ahi1-/- mouse embryonic fibroblasts cells Transcriptomes</description><dates><last_updated>2025-09-24</last_updated><first_public>2022-01-03</first_public></dates><accession>PRJNA730705</accession><cross_references><GEO>GSE174597</GEO><taxon>10090</taxon></cross_references></HashMap>