2020
DOI: 10.20944/preprints202009.0207.v1
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<strong>SMARTdenov</strong><strong>o: A <em>de novo</em> Assembler Using Long Noisy Reads</strong>

Abstract: Long-read single-molecule sequencing has revolutionized de novo genome assembly and enabled the automated reconstruction of reference-quality genomes. It also has been widely used to study structural variants, phase haplotypes and more. Here, we introduce the assembler&mdash; SMARTdenovo, which is an SMS assembler that follows the overlap-layout-consensus (OLC) paradigm. SMARTdenovo (RRID: SCR_017622) was designed to be a fast assembler that did not require highly accurate raw reads for error correction, u… Show more

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Cited by 11 publications
(6 citation statements)
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“…All mapped reads were extracted for the following assemblies. Firstly, we used Canu v1.7 (Koren et al 2017) and SMARTdenovo v1.0.0 (https://github.com/ruanjue/smartde novo) (Liu et al 2020) to generate two primary assemblies.…”
mentioning
confidence: 99%
“…All mapped reads were extracted for the following assemblies. Firstly, we used Canu v1.7 (Koren et al 2017) and SMARTdenovo v1.0.0 (https://github.com/ruanjue/smartde novo) (Liu et al 2020) to generate two primary assemblies.…”
mentioning
confidence: 99%
“…Six recent community-validated assemblers are currently included (Canu [5], [6], Raven [7], MiniAsm [8] (coupled with minipolish [9] for an initial polishing), Shasta [10], smartDeNovo [11]), as well as several tools for polishing (Racon [12] and Pilon [13] for ONT and PB data, Medaka [14] and Nanopolish [15] for ONT data only). If requested, Circlator [16] or a dedicated internal tool can automatically circularise the primary output of assemblers that cannot handle circular molecules (see Supplementary information part 2.2 for more details).…”
Section: Methodsmentioning
confidence: 99%
“…Six recent community-validated assemblers are currently included (Canu [5], Flye [6], Raven [7], MiniAsm [8] (coupled with minipolish [9] for an initial polishing), Shasta [10] and smartDeNovo [11]). Several tools for polishing (Racon [12], Pilon [13], Medaka [14] and Nanopolish [15]) were also included.…”
Section: Methodsmentioning
confidence: 99%
“…The D. huoshanense genome was assembled using PacBio long-read sequencing data, followed by the integration of Illumina paired-end data and Hi-C sequencing data. First, the PacBio sequencing data were de novo assembled into contigs using smartdenovo ( Liu et al. 2020 ) after a correction process with Canu ( Koren et al.…”
Section: Methodsmentioning
confidence: 99%