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  1. ...of ∼27% (3/11). Two other TE-derived peptides, ETVTGVWSY and FLPDHWAVL, were similarly validated in AsPC-1 cells (Fig. 8D). To investigate their genomic and translational origins, we visualized the corresponding chimeric transcripts using the WashU Epi Browser. RNA-seq coverage and getorf-predicted open...
  2. ...(Jang et al. 2019; Shah et al. 2023). Using a combination of SR-RNA-seq and LR-RNA-seq, we created a TE-derived transcript atlas, detailing TE loci with potential promoter activity in different TP53 expression and activation contexts. We found SR-RNA-seq, though robust in transcription quantification...
  3. ...transcripts in a set of cells. By combining standard Illumina-based single-cell RNA-seq quantification of cultured cells’ transcriptomes with PacBio sequencing of the viral transcripts, it was found that this viral genetic variation explained part, but not all, of the heterogeneity in viral gene expression...
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  4. ...(2021) developed a pipeline to quantify RTEs at the transcript level, whereas scTE (He et al. 2021) and IRescue (Polimeni et al. 2024) provide subfamily level quantification of RTEs. Additionally, several tools, including SoloTE (Rodríguez-Quiroz and Valdebenito-Maturana 2022), MATES (Wang et al. 2024...
  5. ...are the gold standard for high-throughput transcriptome profiling (Wang et al. 2009). RNA-sequencing (RNA-seq) has been used to investigate gene expression (The ENCODE Project Consortium 2012), canonical and alternative mRNA splicing (Wright et al. 2022a), noncoding RNAs, and post-transcriptional modifications...
  6. ...et al. 2016; Kuo et al. 2017), our optimized approach improved the performance to enrich genuine full-length transcripts.Our overall results confirm the conclusions from previous studies that the diversity of alternatively spliced isoforms surpasses the current annotation level, even of exceptionally...
  7. ...be increased or reduced through retrotransposition or illegitimate recombination, respectively. LTR sequences proliferate via reverse transcription (Fedoroff 2012), and more active proliferation could increase relative family size in some s. Alternatively, intact LTR elements can be reduced to solo LTRs via...
  8. ...of noise at individual genomic sites.To address this issue, we used a transcript assembly approach that we recently developed (Modzelewski et al. 2021; Shao and Wang 2021). Briefly, we performed transcript assembly using all mapped RNA-seq reads and excluded all annotated protein-coding transcripts. We...
  9. ...–TE transcripts is technically challenging, but long-read transcriptome sequencing will ease many of these difficulties and is therefore a promising avenue for future studies.Using bulk and single-cell RNA-seq to untangle temporal and lineage-specific patterns of TE expression, we observe broadly distinct...
  10. ..., which identified widespread isoform diversity in human neurodevelopment (Jeffries et al. 2020). Advances in long-read sequencing technologies now enable de novo full-transcript assembly and isoform expression quantification, analyses challenging to perform with short-read RNA-seq approaches...
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