2019
DOI: 10.1101/817510
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High quality genome sequence reveals the 12 pseudo-chromosomes of Ganoderma boninense

Abstract: Ganoderma boninense is the dominant fungal pathogen in causing Basal Stem Rot (BSR) disease on oil palm. The whole genome of this fungus was sequenced using PacBio RS II platforms to gain the whole-genome shotgun libraries. These libraries were smoothed with Illumina Hiseq 4000 paired end sequencing to polish the genome assembly. Subsequently, a combination of Dovetail Chicago and HiC libraries with the HiRise assembly pipeline revealed the 12 pseudo-chromosomes of G. boninense. This is the first report of chr… Show more

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Cited by 6 publications
(6 citation statements)
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“…After Hi-C read mapping onto the assembly, generating a draft contact map, and applying automatic reordering of scaffolds in the genome assembly followed by manual correction, more than 85% of the initial genome assembly's scaffolds were successfully grouped into 12 super scaffolds, which are presumed to correspond to the 12 chromosomes of the fungus (Figure 2). This observation aligns with previous findings on the number of chromosomes (12)(13) in other Ganoderma species [40,58,59]. The contact map obtained after reordering, its corresponding labeling, and a table containing the coordinates and sizes of the super scaffolds can be found in Supplementary Files S4-S6, respectively.…”
Section: Improving G Lucidum Genome Assembly Using the Chromosome Con...supporting
confidence: 88%
See 1 more Smart Citation
“…After Hi-C read mapping onto the assembly, generating a draft contact map, and applying automatic reordering of scaffolds in the genome assembly followed by manual correction, more than 85% of the initial genome assembly's scaffolds were successfully grouped into 12 super scaffolds, which are presumed to correspond to the 12 chromosomes of the fungus (Figure 2). This observation aligns with previous findings on the number of chromosomes (12)(13) in other Ganoderma species [40,58,59]. The contact map obtained after reordering, its corresponding labeling, and a table containing the coordinates and sizes of the super scaffolds can be found in Supplementary Files S4-S6, respectively.…”
Section: Improving G Lucidum Genome Assembly Using the Chromosome Con...supporting
confidence: 88%
“…Chromosome conformation capture techniques such as Hi-C have been extensively utilized to significantly enhance the quality of assembled eukaryotic genomes [37], as well as of the microbial genomes from metagenomes [38,39]. However, their utilization in fungal genome research has been relatively scarce, with only one Hi-C-aided Ganoderma genome assembly (G. boninense) published to date [40]. In this study, we obtained a genome assembly for the strain G. lucidum 5.1 by employing a combination of high-throughput shotgun sequencing and the Hi-C method and explored its potential for xylomannan and fucogalactan synthesis.…”
Section: Introductionmentioning
confidence: 99%
“…The 19,851 gene models predicted from PER71 assembly are comparable to G3 with 21,074 coding sequences [27] and G. lucidum with 16,113 genes [28]. Although the number of gene models is higher compared to G. lucidum, 71.30% of PER71 predicted genes are similar to RefSeq proteins.…”
Section: Discussionmentioning
confidence: 99%
“…The genome sequence of the Gb strain G3 was used in this study 32,33 . A fine draft genome sequence was constructed by the hybrid assembly of short reads on the Illumina HiSeq 4000 platform combined with long reads on the PacBio RS II platform to generate a draft genome of this fungus.…”
Section: Global Genome Assembly and Characteristicsmentioning
confidence: 99%