2019
DOI: 10.1038/s41597-019-0139-x
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Chromosome assembly of Collichthys lucidus, a fish of Sciaenidae with a multiple sex chromosome system

Abstract: Collichthys lucidus ( C . lucidus ) is a commercially important marine fish species distributed in coastal regions of East Asia with the X 1 X 1 X 2 X 2 /X 1 X 2 Y multiple sex chromosome system. The karyotype for female C . lucidus is 2n = 48, while 2n = 47 for male ones. … Show more

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Cited by 30 publications
(27 citation statements)
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“…The combination of nanopore long reads and the correction of Illumina short reads ensured the accuracy and completeness of genome assembly, and produced more ideal assembly indexes of contig N50 and less contig number than the genome assembly of several fish species using third-generation sequencing (Table S17) (Gong et al, 2018;Cai et al, 2019;Conte et al, 2019;Ge et al, 2019;He et al, 2019;Jiang et al, 2019; The O. macrolepis genome was annotated to produce 24,770 protein-coding genes (23,991 genes functionally annotated) and…”
Section: Discussionmentioning
confidence: 99%
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“…The combination of nanopore long reads and the correction of Illumina short reads ensured the accuracy and completeness of genome assembly, and produced more ideal assembly indexes of contig N50 and less contig number than the genome assembly of several fish species using third-generation sequencing (Table S17) (Gong et al, 2018;Cai et al, 2019;Conte et al, 2019;Ge et al, 2019;He et al, 2019;Jiang et al, 2019; The O. macrolepis genome was annotated to produce 24,770 protein-coding genes (23,991 genes functionally annotated) and…”
Section: Discussionmentioning
confidence: 99%
“…Our results demonstrate the advantage of nanopore technology. The combination of nanopore long reads and the correction of Illumina short reads ensured the accuracy and completeness of genome assembly, and produced more ideal assembly indexes of contig N50 and less contig number than the genome assembly of several fish species using third‐generation sequencing (Table S17) (Gong et al., 2018; Cai et al., 2019; Conte et al., 2019; Ge et al., 2019; He et al., 2019; Jiang et al., 2019; Yang et al, 2019). Furthermore, physical mappings using Bionano and Hi‐C technology improved greatly the assembly of chromosome‐level genome.…”
Section: Discussionmentioning
confidence: 99%
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“…All raw reads in FASTQ format were filtered using Trimmomatic software (version 0.36; [26]) based on the following criteria: (I) raw reads with sequencing adaptors; (II) a ratio of unidentified nucleotides in the raw reads ≥8%; and (III) raw reads that had more than 50% of base calls with a low quality score (Q<30). After filtering, we downloaded the whole-genome sequence of C. lucidus [27] and used it as a reference sequence for subsequent SNP filtering.…”
Section: Rad Data Processing and Snp Filteringmentioning
confidence: 99%
“…Current sequencing technologies and assembly algorithms change the genome sequencing landscape. Chromosomal assembly can be done through single-molecule sequencing and chromatin conformation capture (3C) data analysis [5][6][7] . PacBio and Illumina sequencing lay the fundamental layer of sequence scaffolds contiguity and resolve repetitive DNA regions 8,9 .…”
Section: Introductionmentioning
confidence: 99%