Highly parallel direct RNA sequencing on an array of nanoporesPublication
Date: 15th January 2018 | Source: Nature Methods
Sequencing the RNA in a biological sample can unlock a wealth of information, including the identity of bacteria and viruses, the nuances of alternative splicing or the transcriptional state of organisms. However, current methods have limitations due to short read lengths and reverse transcription or amplification biases. Here we demonstrate nanopore direct RNA-seq, a highly parallel, real-time, single-molecule method that circumvents reverse transcription or amplification steps. This method yields full-length, strand-specific RNA sequences and enables the direct detection of nucleotide analogs in RNA.
‘Direct RNA sequencing of a human rhinovirus… This approach has many potential advantages over other RNA-Seq strategies’
Garalde et al