<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Data Submission IFOM - ETS</submitter><instrument_platform>NextSeq 550</instrument_platform><study_type>DNA-seq</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16485</full_dataset_link><description>To exclude big genomic variations, we assessed the presence of low-frequency genomic changes using High-depth sequencing.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Cells were collected and washed with PBS 1x and DNA was extracted with the DNeasy Blood &amp; Tissue Kit (Qiagen, 69506). The R26 EYFP locus was amplified by PCR. PCR products were loaded on 1% agarose gel and the bands were purified using the Wizard® SV Gel and PCR Clean-Up System (Promega) according to manufacturer’s instructions.</sample_protocol><sample_protocol>Sequencing - Purified PCR products from mouse cell lines were sequenced with Nextseq 550.</sample_protocol><sample_protocol>Library Construction - The library was prepared with the Illumina DNA Prep kit.</sample_protocol><sample_protocol>Nucleic Acid Extraction - DNeasy Blood and Tissue Kit (Qiagen)</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Data Submission IFOM - ETS</pubmed_authors><pubmed_authors>Sara Tavella</pubmed_authors><pubmed_authors>Fabrizio D'Adda Di Fagagna</pubmed_authors><pubmed_authors>Giovanni Crisafulli</pubmed_authors></additional><is_claimable>false</is_claimable><name>Investigating genomic stability of the R26 EYFP locus in MEFs after Cas9-induced DSB</name><description>To exclude big genomic variations, we assessed the presence of low-frequency genomic changes using High-depth sequencing.</description><dates><release>2026-05-15T00:00:00Z</release><modification>2026-05-15T01:00:41.436Z</modification><creation>2026-01-02T14:47:08.94Z</creation></dates><accession>E-MTAB-16485</accession><cross_references><ENA>ERP187204</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0002693</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>