2020
DOI: 10.1101/2020.07.13.200725
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A high-qualityde novogenome assembly from a single parasitoid wasp

Abstract: Sequencing and assembling a genome with a single individual have several advantages, such as lower heterozygosity and easier sample preparation. However, the amount of genomic DNA of some small sized organisms might not meet the standard DNA input requirement for current sequencing pipelines. Although few studies sequenced a single small insect with about 100 ng DNA as input, it may still be challenging for many small organisms to obtain such amount of DNA from a single individual. Here, we use 20 ng DNA as in… Show more

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Cited by 8 publications
(16 citation statements)
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“…In a recent study, we carrier out the sequencing and assembly of the H. hebetor genomem, its assembled genome is 131.6 Mb in size with a contig N50 of 1.63 Mb (Ye et al, 2020 ). Here, we prepared embryos, larvae, and other samples from the wasps for RNA-Seq analysis.…”
Section: Methodsmentioning
confidence: 99%
“…In a recent study, we carrier out the sequencing and assembly of the H. hebetor genomem, its assembled genome is 131.6 Mb in size with a contig N50 of 1.63 Mb (Ye et al, 2020 ). Here, we prepared embryos, larvae, and other samples from the wasps for RNA-Seq analysis.…”
Section: Methodsmentioning
confidence: 99%
“…We comprehensively considered three factors of each species for comparative genomics analyses and phylogenomic analyses, including genome quality, popularity, and evolutionary position. OrthoFinder v2.5.1 [20] was used to identify the orthologous and paralogous genes of 13 Hymenoptera genomes including O. abietinus (RefSeq assembly accession: GCF_000612105.2), C. chilonis (http://www.insect-genome.com/), Habrobracon hebetor (Ye et al [142]), Trichogramma pertiosum (RefSeq assembly accession: GCF_000599845.2), Nasonia vitripennis (OGS2.0, Rago et al [143]), P. puparum (OGS1.0, Ye et al [13]), G. flavifemur (this study), P. dominula (RefSeq assembly accession: GCF_001465965.1), Solenopsis invicta (RefSeq assembly accession: GCF_000188075.2), Ooceraea biroi (RefSeq assembly accession: GCF_003672135.1), Megachile rotundata (RefSeq assembly accession: GCF_ 000220905.1), A. mellifera (RefSeq assembly accession: GCF_003254395.2), and A. rosae (RefSeq assembly accession: GCF_000344095.2). The basal hymenopteran A. rosae was used as an outgroup.…”
Section: Comparative Genomicsmentioning
confidence: 99%
“…With the development of next-generation sequencing technology, our lab has already completed the sequencing and assembly of the H. hebetor genome and transcriptome. 25,26 In the present study, we employed sgRNA and Cas9 protein by targeting the eye-pigmentation central gene white, which is involved in the transported of pigments, and tested their efficiency in H. hebetor. 27 Eye-color has been the subject of extensive studies mainly due to its ease of use as a marker for genetic transformation in some insects.…”
Section: Introductionmentioning
confidence: 99%