{"title":"Assembly of a Full-Length Chimeric RNA Transcriptome.","authors":"Justin Elfman, Hui Li","doi":"10.1007/978-1-0716-5202-2_5","DOIUrl":null,"url":null,"abstract":"<p><p>Chimeric RNAs are a class of understudied transcripts, characterized by their possession of sequence from two unique annotated parental transcripts. Definitionally, chimeric RNAs exist within gaps in annotation, and most efforts to catalog chimeric RNAs at scale have leveraged short-read paired-end RNAseq. While these have successfully established putative \"chimeromes\" in different tissue and disease contexts, chimeric RNAs predicted via short-read sequencing are defined by the chimeric exon-exon junction, and cannot provide information on the full-length isoforms which contain this junction. These gaps can be remedied by integration of these predictions with full-length, single-molecule, long-read sequencing. In this chapter, we provide instruction on how to integrate long-read sequencing with existing chimeric RNA predictions to establish full-length annotations of long-read transcripts.</p>","PeriodicalId":18490,"journal":{"name":"Methods in molecular biology","volume":"3024 ","pages":"53-60"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods in molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-1-0716-5202-2_5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Chimeric RNAs are a class of understudied transcripts, characterized by their possession of sequence from two unique annotated parental transcripts. Definitionally, chimeric RNAs exist within gaps in annotation, and most efforts to catalog chimeric RNAs at scale have leveraged short-read paired-end RNAseq. While these have successfully established putative "chimeromes" in different tissue and disease contexts, chimeric RNAs predicted via short-read sequencing are defined by the chimeric exon-exon junction, and cannot provide information on the full-length isoforms which contain this junction. These gaps can be remedied by integration of these predictions with full-length, single-molecule, long-read sequencing. In this chapter, we provide instruction on how to integrate long-read sequencing with existing chimeric RNA predictions to establish full-length annotations of long-read transcripts.
期刊介绍:
For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.