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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.
Nanopore sequencing offers real-time, portable, and low-cost DNA sequencing. This review covers computational methods to assess its high error rate and improve data accuracy for applications like base modification detection.
Area of Science:
- Genomics and Bioinformatics
- Molecular Biology
Background:
- Nanopore sequencing is an emerging technology providing real-time, long-read sequencing on portable devices at low cost.
- Despite its advantages, nanopore sequencing is characterized by a high error rate, typically between 5% and 15%, even with recent improvements.
Purpose of the Study:
- To review computational approaches for determining the error rate of nanopore sequencing.
- To outline strategies for improving nanopore sequencing data quality.
Main Methods:
- Literature review of computational methods for nanopore sequencing error rate assessment.
- Analysis of strategies for raw data processing, including base calling and consensus sequence generation.
Main Results:
- Identified and categorized various computational tools and algorithms used to quantify nanopore sequencing errors.
- Highlighted methods for base modification detection and consensus sequence generation from noisy nanopore data.
Conclusions:
- Computational methods are crucial for accurately assessing and mitigating the high error rates in nanopore sequencing.
- Effective data processing strategies can translate raw nanopore reads into reliable base calls, enabling diverse research applications and base modification detection.
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