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Sequencing of mRNA from Whole Blood using Nanopore Sequencing
Published on: June 3, 2019
From squiggle to basepair: computational approaches for improving nanopore sequencing read accuracy
Franka J Rang1, Wigard P Kloosterman2, Jeroen de Ridder3
1Department of Genetics, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, 3584, CG, Utrecht, The Netherlands.
Abstract:
Nanopore sequencing is a rapidly maturing technology delivering long reads in real time on a portable instrument at low cost. Not surprisingly, the community has rapidly taken up this new way of sequencing and has used it successfully for a variety of research applications. A major limitation of nanopore sequencing is its high error rate, which despite recent improvements to the nanopore chemistry and computational tools still ranges between 5% and 15%. Here, we review computational approaches determining the nanopore sequencing error rate. Furthermore, we outline strategies for translation of raw sequencing data into base calls for detection of base modifications and for obtaining consensus sequences.
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