2017
DOI: 10.12688/f1000research.11354.1
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MinION Analysis and Reference Consortium: Phase 2 data release and analysis of R9.0 chemistry

Abstract: Background: Long-read sequencing is rapidly evolving and reshaping the suite of opportunities for genomic analysis. For the MinION in particular, as both the platform and chemistry develop, the user community requires reference data to set performance expectations and maximally exploit third-generation sequencing. We performed an analysis of MinION data derived from whole genome sequencing of K-12 using the R9.0 chemistry, Escherichia coli comparing the results with the older R7.3 chemistry. Methods: We comput… Show more

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Cited by 116 publications
(79 citation statements)
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“…2a) for most positions, with increased deletions toward the 5' end due to increased steric hindrance as strand length increases [10]. Literature suggests a nanopore error rate near 10% [8,11], so we also performed a synthesis-to-sequencing error rate analysis on an 89-mer hairpin sequence, encoding "HELLO" in its first 32 payload bases. Figure 2b shows the read error when aligned to the extended adapter and payload sequence.…”
Section: Mainmentioning
confidence: 99%
“…2a) for most positions, with increased deletions toward the 5' end due to increased steric hindrance as strand length increases [10]. Literature suggests a nanopore error rate near 10% [8,11], so we also performed a synthesis-to-sequencing error rate analysis on an 89-mer hairpin sequence, encoding "HELLO" in its first 32 payload bases. Figure 2b shows the read error when aligned to the extended adapter and payload sequence.…”
Section: Mainmentioning
confidence: 99%
“…À l'issue de ce processus d'amélioration, cette technique, commercialisée par Oxford Nanopore Technologies [17,48] (➜) et fondée sur des pores biologiques et la détec-tion électrique, permet d'extraire la séquence de longs fragments individuels de 10 à 1 000 kb, ce qui autorise la compensation par redondance d'un taux d'erreur total élevé. Le taux d'erreur brut total est, dans le meilleur des cas, de 7,5 % pour la lecture d'une base individuelle chez E. coli, en comptant erreurs, insertions et délétions [18]. En utilisant des méthodes par consensus (redondance), la précision progresse jusqu'à 99,5 %, pour une couverture de 30 fois la longueur du génome chez la bactérie E. coli [19].…”
Section: Séquençage De L'adn Par Nanopores Résultats Et Perspectivesunclassified
“…En utilisant des méthodes par consensus (redondance), la précision progresse jusqu'à 99,5 %, pour une couverture de 30 fois la longueur du génome chez la bactérie E. coli [19]. La vitesse de lecture est, par nanopore, de 250 à 450 bases par seconde [13,18]. La parallélisation est plus faible que celle obtenue par les techniques d'amplification actuelles (512 à 144 000 pores en parallèle, selon le modèle, et aureus) permettait de forcer des macromolécules (ADN et ARN simple brin) à transiter par cette nano-cavité.…”
Section: Séquençage De L'adn Par Nanopores Résultats Et Perspectivesunclassified
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“…The Oxford Nanopore Technologies (ONT) MinION sequencer is currently the only available portable sequencer. Although nanopore sequencing is known to have higher raw sequence error rates in comparison to standard short read sequencing platforms such as Illumina or BGI-Seq, particularly at homopolymeric regions (Ip et al, 2015;Jain et al, 2017), significant improvements in the accuracy of MinION sequencing chemistry has led to its recent rise in popularity for field applications (reviewed in Srivathsan et al, 2019). This sequencer is especially useful in situations where there is a lack of access to sequencing facilities or when sample export is difficult.…”
Section: Introductionmentioning
confidence: 99%