2021
DOI: 10.3389/fgene.2021.747552
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Chromosome-Level Genome Assembly of the Burbot (Lota lota) Using Nanopore and Hi-C Technologies

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Cited by 5 publications
(3 citation statements)
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“…The chromosome-level genome assemblies generated, corresponded to the numbers of chromosomes reported from cytogenetic studies (see Table S1), except for burbot where we obtained a total of n=23 haploid chromosomes vs. n=24 haploid chromosomes reported by two different cytogenetic studies [40,41]. We cannot rule out resulting in n=24 chromosomes [52]. Combined, these results suggest that there are chromosomal differences between different lineages of burbot.…”
Section: Chromosome Number Variability In Codfishesmentioning
confidence: 70%
See 1 more Smart Citation
“…The chromosome-level genome assemblies generated, corresponded to the numbers of chromosomes reported from cytogenetic studies (see Table S1), except for burbot where we obtained a total of n=23 haploid chromosomes vs. n=24 haploid chromosomes reported by two different cytogenetic studies [40,41]. We cannot rule out resulting in n=24 chromosomes [52]. Combined, these results suggest that there are chromosomal differences between different lineages of burbot.…”
Section: Chromosome Number Variability In Codfishesmentioning
confidence: 70%
“…Moreover, two different chromosome-level burbot assemblies have previously been constructed, which resulted in different numbers of chromosomes, one by Han et al 2021 of a specimen sampled in Heilong River (Raohe county) in the northeastern part of China resulting in n=22 chromosomes[51], and another by Song et al 2021 resulting in n=24 chromosomes[52]. Combined, these results suggest that there are chromosomal differences between different lineages of burbot.…”
Section: Discussionmentioning
confidence: 99%
“…Three years later, also using the PacBio long-read and NGS data, the reference of the Indian rhesus macaque (Mmul_10) was improved significantly (∼120-fold) in sequence contiguity (46Mb of contig N50) relative to rheMac8 [19]. In recent years, another big step forward for de novo genome assembly comes from the development of the Nanopore long-read sequencing with its cost-effective advantage [36, 37], which improved the genome references for multiple species, such as humans [38-41], mammals [42-44], birds [45, 46], plants [47-49], fishes [50, 51], fruit flies [52], etc. However, there is still no nanopore derived reference assembly and related analyses (such as methylation, recombination rate, etc.)…”
Section: Introductionmentioning
confidence: 99%