2019
DOI: 10.1186/s12859-019-3114-9
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SLR: a scaffolding algorithm based on long reads and contig classification

Abstract: BackgroundScaffolding is an important step in genome assembly that orders and orients the contigs produced by assemblers. However, repetitive regions in contigs usually prevent scaffolding from producing accurate results. How to solve the problem of repetitive regions has received a great deal of attention. In the past few years, long reads sequenced by third-generation sequencing technologies (Pacific Biosciences and Oxford Nanopore) have been demonstrated to be useful for sequencing repetitive regions in gen… Show more

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Cited by 25 publications
(16 citation statements)
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“…Validated paired-end reads were also used to calculate interchromosomal interactions to analyze chromosome territories. The contigs were further independently assembled into scaffolds using SLR (Luo et al, 2019) and SALSA (Ghurye et al, 2017), respectively, to validate the accuracy of the LACHESIS assembly.…”
Section: Chromosomal Genome Assembly and Chromatin Interactions Using Hi-c Technologymentioning
confidence: 99%
“…Validated paired-end reads were also used to calculate interchromosomal interactions to analyze chromosome territories. The contigs were further independently assembled into scaffolds using SLR (Luo et al, 2019) and SALSA (Ghurye et al, 2017), respectively, to validate the accuracy of the LACHESIS assembly.…”
Section: Chromosomal Genome Assembly and Chromatin Interactions Using Hi-c Technologymentioning
confidence: 99%
“…Hybrid assemblies of Illumina and Nanopore reads were constructed for each symbiont genome with SPA des (Gamma1) (56) or meta SPA des (all others) (57) choosing k-mers between 21 and 91 in 10 step increments. Raw assemblies for the Epsilon, Gamma1 and Ifr-SOX symbionts were binned with GBT ools (58) and incrementally gap filled, corrected and scaffolded with LR_G ap C loser (59), ra2.py (60), and SLR (61), respectively, following recommendations by (62) The Ifr-MOX symbiont assembly was automatically binned with M eta BAT2 (63) for contigs ≧ 1500 bp. Shorter contigs (≧ 500 bp) were binned with M ax B in (64).…”
Section: Methodsmentioning
confidence: 99%
“…The genome assembly was then phased using the Purge Haplotigs v. 1.1.1 pipeline 59 . Scaffolding of the assembled sequences was undertaken with SLR v. 1.0 60 using the NECAT corrected long-read MinION data set. SLR was run with default settings.…”
Section: Methodsmentioning
confidence: 99%