<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(4)</volume><submitter>Lv W</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Extrachromosomal circular deoxyribonucleic acid (eccDNA) is evolving as a valuable biomarker, while little is known about its presence in urine.&lt;h4>Methods&lt;/h4>Here, we report the discovery and analysis of urinary cell-free eccDNAs (ucf-eccDNAs) in healthy controls and patients with advanced chronic kidney disease (CKD) by Circle-Seq.&lt;h4>Results&lt;/h4>Millions of unique ucf-eccDNAs were identified and comprehensively characterised. The ucf-eccDNAs are GC-rich. Most ucf-eccDNAs are less than 1000 bp and are enriched in four pronounced peaks at 207, 358, 553 and 732 bp. Analysis of the genomic distribution of ucf-eccDNAs shows that eccDNAs are found on all chromosomes but enriched on chromosomes 17, 19 and 20 with a high density of protein-coding genes, CpG islands, short in</pubmed_abstract><journal>Clinical and translational medicine</journal><pagination>e817</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9042798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Circle-Seq reveals genomic and disease-specific hallmarks in urinary cell-free extrachromosomal circular DNAs.</pubmed_title><pmcid>PMC9042798</pmcid><pubmed_authors>Han P</pubmed_authors><pubmed_authors>Lv W</pubmed_authors><pubmed_authors>Bolund L</pubmed_authors><pubmed_authors>Qu K</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Pan X</pubmed_authors><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>He F</pubmed_authors><pubmed_authors>Jin X</pubmed_authors><pubmed_authors>Yin T</pubmed_authors><pubmed_authors>Xing X</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Zheng T</pubmed_authors><pubmed_authors>Regenberg B</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Henriksen RA</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Luo Y</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Lin L</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Circle-Seq reveals genomic and disease-specific hallmarks in urinary cell-free extrachromosomal circular DNAs.</name><description>&lt;h4>Background&lt;/h4>Extrachromosomal circular deoxyribonucleic acid (eccDNA) is evolving as a valuable biomarker, while little is known about its presence in urine.&lt;h4>Methods&lt;/h4>Here, we report the discovery and analysis of urinary cell-free eccDNAs (ucf-eccDNAs) in healthy controls and patients with advanced chronic kidney disease (CKD) by Circle-Seq.&lt;h4>Results&lt;/h4>Millions of unique ucf-eccDNAs were identified and comprehensively characterised. The ucf-eccDNAs are GC-rich. Most ucf-eccDNAs are less than 1000 bp and are enriched in four pronounced peaks at 207, 358, 553 and 732 bp. Analysis of the genomic distribution of ucf-eccDNAs shows that eccDNAs are found on all chromosomes but enriched on chromosomes 17, 19 and 20 with a high density of protein-coding genes, CpG islands, short in</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-05T13:23:25.25Z</modification><creation>2025-04-05T13:23:25.25Z</creation></dates><accession>S-EPMC9042798</accession><cross_references><pubmed>35474296</pubmed><doi>10.1002/ctm2.817</doi></cross_references></HashMap>