Searching journal content for articles similar to Choquet et al. 35 (4): 712.

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  1. ...direct RNA-seq method can potentially overcome these issues while also identifying RNA modifications in the native molecule. However, sequencing throughput from current direct RNA protocols is still relatively low compared to cDNA-based protocols (∼20 M reads in direct RNA protocols [Oxford Nanopore...
  2. ...fall in introns; thus, these reads likely represent mature mRNA molecules rather than DNA contamination, and 5′ truncation may occur during library preparation, sequencing, or processing of the data. The presence of truncation is also supported by the relatively shorter reads generated by ONT directRNA...
  3. ...and ligates the exon sequences together to generate translation-competent mRNA (Wang et al. 2015). Conserved sequences at exon–intron boundaries (splice sites) direct spliceosome assembly on each newly synthesized intron. The spliceosome can assemble different combinations of exon sequences to generate mRNA...
  4. ...probability assessment using the direct RNA nanopore sequencing of the 5EU-containing synthetic RNAs showed that RNAs are recognizable as 5EU containing with a probability of 0.75 once a minimum length of 500 nt is reached (Supplemental Fig. S1C). This covers the vast majority (93%) of all mature RNAs...
  5. ...based on the integrative analysis of total and nascent transcription, the latter being quantified through RNA metabolic labeling. We developed INSPEcT−, a computational method based on the mathematical modeling of premature and mature RNA expression that is able to quantify kinetic rates from steady...
  6. ...). This effectively means that, for the entire duration of S phase, two copies of a gene that replicated early produce as much mRNA as one copy had been producing before replication. Our findings on the kinetics of nucleosome positioning maturation, which suggest that one replicated gene copy is more expressed than...
  7. ...leverage mutants that ablate NMD, the sensitivity of short-read RNA sequencing, and the unique information captured by long-read, nanopore direct RNA sequencing. Using a modified nanopore sequencing protocol, we capture isoform, decapping/cleavage site, and poly(A) tail information for individual, native mRNA...
  8. ...(A) signal evolved in eukaryotes, we explored poly(A) signals in other eukaryotic species. Although our initial experiments with G. lamblia assemblage A used both short and long-read sequences to identify poly(A) signals (Bilodeau et al. 2022), we reasoned that direct RNA Oxford Nanopore Technology would...
  9. ...transposons introduce cryptic splice sites into the nascent transcript and thereby significantly expand the neural transcript repertoire. Some genes exclusively produce chimeric mRNAs with transposon sequence; on average, 11.6% of the mRNAs produced from a given gene are chimeric. Conversely, most transposon...
  10. ...of circRNAs, can be used to identify exonic, intronic, and intergenic circRNAs (Zheng et al. 2019). CYCLeR constructs a splice graph based on the alignment and can also capture the full-length sequences of circRNAs (Stefanov and Meyer 2023). Oxford Nanopore Technology (ONT) sequencing has also been...
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