{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Satou Y"],"funding":["Canadian Institutes of Health Research"],"pagination":["R152"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2760879"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["9(10)"],"pubmed_abstract":["<h4>Background</h4>The draft genome sequence of the ascidian Ciona intestinalis, along with associated gene models, has been a valuable research resource. However, recently accumulated expressed sequence tag (EST)/cDNA data have revealed numerous inconsistencies with the gene models due in part to intrinsic limitations in gene prediction programs and in part to the fragmented nature of the assembly.<h4>Results</h4>We have prepared a less-fragmented assembly on the basis of scaffold-joining guided by paired-end EST and bacterial artificial chromosome (BAC) sequences, and BAC chromosomal in situ hybridization data. The new assembly (115.2 Mb) is similar in length to the initial assembly (116.7 Mb) but contains 1,272 (approximately 50%) fewer scaffolds. The largest scaffold in the new assembl"],"journal":["Genome biology"],"pubmed_title":["Improved genome assembly and evidence-based global gene model set for the chordate Ciona intestinalis: new insight into intron and operon populations."],"pmcid":["PMC2760879"],"funding_grant_id":["MOP-77708"],"pubmed_authors":["Roe BA","Hastings KE","Wasserscheid J","Hotta K","Inaba K","Satou Y","Mineta K","Dewar K","Shoguchi E","Wiley GB","Yamada L","Lemaire P","Macmil SL","Ueno K","Ogasawara M","Sasakura Y","Endo T","Zeller RW","Matsumoto J","Lindquist E"],"additional_accession":[]},"is_claimable":false,"name":"Improved genome assembly and evidence-based global gene model set for the chordate Ciona intestinalis: new insight into intron and operon populations.","description":"<h4>Background</h4>The draft genome sequence of the ascidian Ciona intestinalis, along with associated gene models, has been a valuable research resource. However, recently accumulated expressed sequence tag (EST)/cDNA data have revealed numerous inconsistencies with the gene models due in part to intrinsic limitations in gene prediction programs and in part to the fragmented nature of the assembly.<h4>Results</h4>We have prepared a less-fragmented assembly on the basis of scaffold-joining guided by paired-end EST and bacterial artificial chromosome (BAC) sequences, and BAC chromosomal in situ hybridization data. The new assembly (115.2 Mb) is similar in length to the initial assembly (116.7 Mb) but contains 1,272 (approximately 50%) fewer scaffolds. The largest scaffold in the new assembl","dates":{"release":"2008-01-01T00:00:00Z","publication":"2008 Oct","modification":"2026-04-07T15:17:38.644Z","creation":"2026-04-07T14:36:11.57Z"},"accession":"S-EPMC2760879","cross_references":{"pubmed":["18854010"],"doi":["10.1186/gb-2008-9-10-r152"]}}