2021
DOI: 10.1016/j.ijbiomac.2020.12.098
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Characterization and analysis of the transcriptome in Opisina arenosella from different developmental stages using single-molecule real-time transcript sequencing and RNA-seq

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Cited by 9 publications
(15 citation statements)
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“…Although the high-quality reference genome has been released in 2019 ( Kawamoto et al, 2019 ), the transcriptome so far was obtained through assembling short reads resulting in poor-quality transcripts and incorrect genome annotation ( Shao et al, 2012 ; Suetsugu et al, 2013 ). Recently, with the development of sequencing technology, PacBio sequencing, which has a profound advantage in long reads, has been applied widely to generate high-quality full-length transcripts in eukaryotes ( Sharon et al, 2013 ; Wang et al, 2016 ; Jiang et al, 2019 ; Wang et al, 2019 ; Yang et al, 2020 ; Xu et al, 2021 ). In this study, we identified 25,970 high-quality transcripts in the silkworm by using PacBio sequencing technology.…”
Section: Discussionmentioning
confidence: 99%
“…Although the high-quality reference genome has been released in 2019 ( Kawamoto et al, 2019 ), the transcriptome so far was obtained through assembling short reads resulting in poor-quality transcripts and incorrect genome annotation ( Shao et al, 2012 ; Suetsugu et al, 2013 ). Recently, with the development of sequencing technology, PacBio sequencing, which has a profound advantage in long reads, has been applied widely to generate high-quality full-length transcripts in eukaryotes ( Sharon et al, 2013 ; Wang et al, 2016 ; Jiang et al, 2019 ; Wang et al, 2019 ; Yang et al, 2020 ; Xu et al, 2021 ). In this study, we identified 25,970 high-quality transcripts in the silkworm by using PacBio sequencing technology.…”
Section: Discussionmentioning
confidence: 99%
“…The RNA was transformed into cDNA using the Hiscript III Reverse Transcription Kit (Vazyme, Nanjing, China), and fluorescent quantitative PCR was performed on an ABI 7500 (Thermo, MA, United Sttaes) using the AceQ qPCR SYBR Green Master Mix system (Vazyme, Nanjing, China). The relative quantitative 2 −ΔΔCt method was used to analyze genes expression ( Xu et al, 2021 ).…”
Section: Methodsmentioning
confidence: 99%
“…Eighteen samples (AhWr1, AhWr2, AhWr3; AhWs1, AhWs2, AhWs3; AhWf1, AhWf2, AhWf3; AhCr1, AhCr2, AhCr3; AhCs1, AhCs2, AhCs3; AhCf1, AhCf2, and AhCf3) were used for RNA extraction, and total RNA from the 18 samples was used for Illumina sequencing. For SMRT sequencing, total RNA from the 18 samples was mixed for subsequent experiments, according to previous studies [49][50][51][52].…”
Section: Plant Materialsmentioning
confidence: 99%