{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["14"],"submitter":["Wenger Y"],"pubmed_abstract":["<h4>Background</h4>Evolutionary studies benefit from deep sequencing technologies that generate genomic and transcriptomic sequences from a variety of organisms. Genome sequencing and RNAseq have complementary strengths. In this study, we present the assembly of the most complete Hydra transcriptome to date along with a comparative analysis of the specific features of RNAseq and genome-predicted transcriptomes currently available in the freshwater hydrozoan Hydra vulgaris.<h4>Results</h4>To produce an accurate and extensive Hydra transcriptome, we combined Illumina and 454 Titanium reads, giving the primacy to Illumina over 454 reads to correct homopolymer errors. This strategy yielded an RNAseq transcriptome that contains 48'909 unique sequences including splice variants, representing app"],"journal":["BMC genomics"],"pagination":["204"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3764976"],"repository":["biostudies-literature"],"pubmed_title":["RNAseq versus genome-predicted transcriptomes: a large population of novel transcripts identified in an Illumina-454 Hydra transcriptome."],"pmcid":["PMC3764976"],"pubmed_authors":["Galliot B","Wenger Y"],"additional_accession":[]},"is_claimable":false,"name":"RNAseq versus genome-predicted transcriptomes: a large population of novel transcripts identified in an Illumina-454 Hydra transcriptome.","description":"<h4>Background</h4>Evolutionary studies benefit from deep sequencing technologies that generate genomic and transcriptomic sequences from a variety of organisms. Genome sequencing and RNAseq have complementary strengths. In this study, we present the assembly of the most complete Hydra transcriptome to date along with a comparative analysis of the specific features of RNAseq and genome-predicted transcriptomes currently available in the freshwater hydrozoan Hydra vulgaris.<h4>Results</h4>To produce an accurate and extensive Hydra transcriptome, we combined Illumina and 454 Titanium reads, giving the primacy to Illumina over 454 reads to correct homopolymer errors. This strategy yielded an RNAseq transcriptome that contains 48'909 unique sequences including splice variants, representing app","dates":{"release":"2013-01-01T00:00:00Z","publication":"2013 Mar","modification":"2026-05-30T09:49:57.805Z","creation":"2019-03-27T01:15:39Z"},"accession":"S-EPMC3764976","cross_references":{"pubmed":["23530871"],"doi":["10.1186/1471-2164-14-204"]}}