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2018
DOI: 10.1101/452870
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Divergent selection causes whole genome differentiation without physical linkage among the targets in Spodoptera frugiperda (Noctuidae)

Abstract: 1 2 3 4 5 6 7 8 9 10 11 12 1 ABSTRACTThe process of speciation involves whole genome differentiation by overcoming gene flow between diverging populations. We have ample knowledge which evolutionary forces may cause genomic differentiation, and several speciation models have been proposed to explain the transition from genetic to genomic differentiation. However, it is still unclear what are critical conditions enabling genomic differentiation in nature. The Fall armyworm, Spodoptera frugiperda, is observed as… Show more

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Cited by 9 publications
(17 citation statements)
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“…Then, Dovetail™ Hi-C library was constructed from this strain, followed by Illumina Hiseq-X sequencing. Then, we used Hi-Rise™ software 24 to perform scaffolding from a PacBio genome assembly 22 , which was generated from individuals from the same insectarium. Then, the gene annotation was also transferred from this PacBio genome assembly to newly scaffoled-assembly.…”
Section: Methods Datamentioning
confidence: 99%
See 2 more Smart Citations
“…Then, Dovetail™ Hi-C library was constructed from this strain, followed by Illumina Hiseq-X sequencing. Then, we used Hi-Rise™ software 24 to perform scaffolding from a PacBio genome assembly 22 , which was generated from individuals from the same insectarium. Then, the gene annotation was also transferred from this PacBio genome assembly to newly scaffoled-assembly.…”
Section: Methods Datamentioning
confidence: 99%
“…The resequencing data from the MS was obtained from NCBI SRA (PRJNA494340), which was generated for the fall armyworm genome project 10 and speciation study 22 . For PR, we collected larvae samples at Santa Isabella (see 38 for more detail).…”
Section: Methods Datamentioning
confidence: 99%
See 1 more Smart Citation
“…Further quality control and confirmation that adapter and non-relevant (contaminants, primer artifacts) sequences were removed from filtered reads were performed using FastQC [35]. Given the prevalence of C-strain among our samples and similar number of variants called when using both S. frugiperda corn and rice genomes [36], we mapped the remaining reads to the S. frugiperda corn reference genome (v3.1) downloaded from https://bipaa.genouest.org/sp/spodoptera_frugiperda_pub/ (assembled length of 312 Mb across 29,949 scaffolds [17]) using a Burrows-Wheeler aligner algorithm (bwa-mem) [37]. Variants were then called using the SAMtools mpileup utility [38], resulting in detection of 126,977,977 single nucleotide polymorphisms (SNPs) and indels.…”
Section: Filtering and Mappingmentioning
confidence: 99%
“…with ~20X coverage was used to perform whole genome resequencing with 150bp paired-end and 300bp insert length. Then, we combined the resequencing data from Puerto Rico and Mississippi, which were generated for our previous studies (Hiseq 2500, Hiseq 4000, and Novaseq 6000) 31,32 , as well as the resequencing data of Brazil, Malawi, and Uganda from CSIRO (Novaseq 6000, 150bp paired-end sequencing) 28 . Lastly, resequencing data from China 33 was also combined with the dataset.…”
Section: Genome Assemblymentioning
confidence: 99%