<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/SRR125/082/SRR12570082/SRR12570082_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/080/SRR12570080/SRR12570080_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/083/SRR12570083/SRR12570083_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/078/SRR12570078/SRR12570078_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/081/SRR12570081/SRR12570081.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/078/SRR12570078/SRR12570078.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/079/SRR12570079/SRR12570079_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/080/SRR12570080/SRR12570080_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/082/SRR12570082/SRR12570082_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/078/SRR12570078/SRR12570078_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/079/SRR12570079/SRR12570079_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/083/SRR12570083/SRR12570083_1.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>anhui university</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA661030</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>In previous study, we found circFAT1(e2) was highly expressed in breast cancer tissues and cell lines. And this factor is also a crucial role in breast cancer genesis and development. So in this study, we knocked down circFAT1(e2) in MCF-7 cells. The viability and metastasis was significantly inhibited with circFAT1(e2) depletion. In order to explore the potential down-stream gene of circFAT1(e2) in breast cancer cells. We extracted the total RNA from circFAT1(e2) knockdown MCF-7 cells and negative control group by using TriZol reagent. Then, toal RNA was subjected to transcriptome sequencing to determine the potential down-stream targets of circFAT1(e2). We expect to reveal the underlied mechanism of the regulatory effect on breast cancer of circFAT1(e2). Overall design: CircFAT1(e2) was knocked down in siZ5 group to identify the down-stream genes of this circRNA in MCF-7 cell, and siNC was used as a knockdown control in this experiment.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Transcriptome analysis of gene expression in MCF-7 cell upon circFAT1(e2) depletion</name><description>Transcriptome analysis of gene expression in MCF-7 cell upon circFAT1(e2) depletion</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-01-27</first_public></dates><accession>PRJNA661030</accession><cross_references><GEO>GSE157343</GEO><taxon>9606</taxon></cross_references></HashMap>