Determining Exon Connectivity in Complex mRNAs by Nanopore Sequencing

BioRxiv : the Preprint Server for Biology
Mohan T BolisettyBrenton R Graveley

Abstract

Though powerful, short-read high throughput RNA sequencing is limited in its ability to directly measure exon connectivity in mRNAs containing multiple alternative exons located farther apart than the maximum read lengths. Here, we use the Oxford Nanopore MinION™ sequencer to identify 7,899 ‘full-length’ isoforms expressed from four Drosophila genes, Dscam1, MRP, Mhc, and Rdl. These results demonstrate that nanopore sequencing can be used to deconvolute individual isoforms and that it has the potential to be an important method for comprehensive transcriptome characterization.

Related Concepts

Antigens, Tumor-Associated, Carbohydrate
Drosophila
Exons
Genes
Major Histocompatibility Complex
RNA, Messenger
Protein Isoforms
High Throughput Analysis
Protein Expression
Nucleic Acid Sequencing

Related Feeds

BioRxiv & MedRxiv Preprints

BioRxiv and MedRxiv are the preprint servers for biology and health sciences respectively, operated by Cold Spring Harbor Laboratory. Here are the latest preprint articles (which are not peer-reviewed) from BioRxiv and MedRxiv.