<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/ERR499/001/ERR4992201/ERR4992201_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/002/ERR4992202/ERR4992202_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/000/ERR4992200/ERR4992200_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/005/ERR4992205/ERR4992205_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/003/ERR4992203/ERR4992203_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/002/ERR4992202/ERR4992202_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/005/ERR4992205/ERR4992205_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/004/ERR4992204/ERR4992204_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/001/ERR4992201/ERR4992201_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/003/ERR4992203/ERR4992203_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/004/ERR4992204/ERR4992204_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR499/000/ERR4992200/ERR4992200_2.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>European Bioinformatics Institute</center_name><center_name>Department of Biology Southern University of Science and Technology</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJEB42003</full_dataset_link><broker_name>ArrayExpress</broker_name><long_description>Here, we systematically investigated circRNAs in the APP/PS1 model mouse brain through deep RNA-sequencing. We report that circRNAs are markedly enriched in the brain and that several circRNAs exhibit differential expression between wild-type and APP/PS1 mice. We characterized one abundant circRNA, circTulp4, derived from Intron1 of the gene Tulp4. To investigate the effect of CircTulp4 on chromatin status, we used ATAC-seq to investigate the chromatin accessibility upon CircTulp4 knockdown.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>CircTulp4 functions in Alzheimer’s disease pathogenesis by regulating its parental gene Tulp4</name><description>CircTulp4 functions in Alzheimer’s disease pathogenesis by regulating its parental gene Tulp4</description><dates><last_updated>2020-12-15</last_updated><first_public>2021-03-01</first_public></dates><accession>PRJEB42003</accession><cross_references/></HashMap>