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Transcript Profiling Using Long-Read Sequencing Technologies

Authors :
Yu Chang Wang
Jiannis Ragoussis
Spyros Oikonomopoulos
Haig Djambazian
Somayyeh Fahiminiya
Anthony Bayega
Source :
Methods in Molecular Biology ISBN: 9781493978335
Publication Year :
2018
Publisher :
Springer New York, 2018.

Abstract

RNA sequencing using next-generation sequencing (NGS, RNA-Seq) technologies is currently the standard approach for gene expression profiling, particularly for large-scale high-throughput studies. NGS technologies comprise short-read RNA-Seq (dominated by Illumina) and long-read RNA-Seq technologies provided by Pacific Bioscience (PacBio) and Oxford Nanopore Technologies (ONT). Although short-read sequencing technologies are the most widely used, long-read technologies are increasingly becoming the standard approach for de novo transcriptome assembly and isoform expression quantification due to the complex nature of the transcriptome which consists of variable lengths of transcripts and multiple alternatively spliced isoforms for most genes. In this chapter, we describe experimental procedures for library preparation, sequencing, and associated data analysis approaches for PacBio and ONT with a major focus on full length cDNA synthesis, de novo transcriptome assembly, and isoform quantification.

Details

ISBN :
978-1-4939-7833-5
ISBNs :
9781493978335
Database :
OpenAIRE
Journal :
Methods in Molecular Biology ISBN: 9781493978335
Accession number :
edsair.doi...........88b7cdc4f812decec76384ec9c6d870b
Full Text :
https://doi.org/10.1007/978-1-4939-7834-2_6