Nature GeneticsGenomicsPeer-reviewed journal article
High-throughput annotation of full-length long noncoding RNAs with Capture Long-Read Sequencing
Julien LagardeiD, Barbara Uszczyńska-RatajczakiD, Silvia Carbonell, Sílvia Pérez-LluchiD, Amaya AbadiD, Carrie Davis, T GingerasiD, Adam FrankishiD, Jennifer HarrowiD, Roderic GuigóiD, Rory JohnsoniD
Abstract
Accurate annotations of genes and their transcripts is a foundation of genomics, but no annotation technique presently combines throughput and accuracy. As a result, reference gene collections remain incomplete: many gene models are fragmentary, while thousands more remain uncatalogued-particularly for long noncoding RNAs (lncRNAs). To accelerate lncRNA annotation, the GENCODE consortium has developed RNA Capture Long Seq (CLS), combining targeted RNA capture with third-generation long-read sequencing. We present an experimental re-annotation of the GENCODE intergenic lncRNA population in matched human and mouse tissues, resulting in novel transcript models for 3574 / 561 gene loci, respectively. CLS approximately doubles the annotated complexity of targeted loci, outperforming existing short-read techniques. Full-length transcript models produced by CLS enable us to definitively characterize the genomic features of lncRNAs, including promoter- and gene-structure, and protein-coding potential. Thus CLS removes a longstanding bottleneck of transcriptome annotation, generating manual-quality full-length transcript models at high-throughput scales.\n\nAbbreviations
- organism: human
- organism: mouse
- assay: long-read sequencing
- research focus: cell type annotation
- research focus: gene regulatory network inference
- research focus: database / resource
- approach: experimental assay
- Citations
- 267
- FWCI
- 12.06
- Field percentile
- top 1%
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