Searching journal content for articles similar to de Hoon et al. 32 (9): 1727.

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  1. ...of operative transcription factors (TFs). However, identification of conserved CRMs is often 61 confounded by rearrangement and substitution of TFBSs, leading to similar functional 62 capabilities without deep sequence conservation (reviewed in (Nelson and Wardle 2013; Long 63 et al. 2016; Jindal and Farley...
  2. ...ORFs, results from the altered ribosome footprint length at the codon preceding the stop codon (Wu et al. 2024a).Third example: translation of noncoding RNATAS3 is an annotated noncoding RNA, encoding the primary transcript of trans-acting short-interfering RNA (tasiRNA). A small ORF is known to be translated...
  3. ...studies have provided insights into the complexity of alternative isoforms at a deep evolutionary timescale. However, the diversity and pattern of the alternative isoform landscape within natural populations remain largely unexplored (Verta and Jacobs 2022).Owing to its well-defined evolutionary history...
  4. ...proband contigs was 29.05 Mb (Table 1).View this table: In this window In a new window Table 1. Demographics, and sequencing and assembly metrics for the cohortHiFi reads were aligned to hg38, and variant calling was performed using DeepVariant (Poplin et al. 2018) and pbsv (https...
  5. ...transcriptome is highly complex and includes RNAs that potentially hybridize to form double-stranded RNA (dsRNA). We isolated dsRNA using the monoclonal J2 antibody and deep-sequenced the enriched samples from testes of juvenile Dicer1 knockout mice, age-matched controls, and adult animals. Comparison of our...
  6. ...concordant with TSS peaks called by RAMPAGE, CAGE-seq, and GRO-cap signals using human cancer cell lines. In addition, robust long-read full-length RNA-seq has the advantage of trivially identifying alternative transcripts. Previous studies have also shown that long-read sequencing can identify thousands...
  7. ...” and “UACUCC” IRES elements, and novel short C/U-related sequences (such as “CCCUCUU” and “UUCCUU) that can base pair with 18S rRNAs within a scanning ribosome to enhance cap-independent translation (Weingarten-Gabbay et al. 2016). However, much less evidence is available for their regulatory roles in plant mRNA...
  8. ...d of continuous proliferation (Fig. 1A). Deep sequencing was used to quantify sgRNA representation at each time point. After normalization and mean-variance modeling, we determined enriched and depleted sgRNAs (Fig. 1B). The experiment was performed in technical and biological duplicates, which both...
  9. ...were generated using deepTools (Ramírez et al. 2016). The ATAC-inferred CTCF-bound sites per tissue were used to calculate LOR for TE subfamily enrichment. To test the significance of TE subfamily enrichment in a specific tissue for certain epigenetic states, we binned the reference into 100-bp...
  10. ...transcripts. Although the heterogeneity of pre-mRNA 3′ end processing has been established with high-throughput approaches, the mechanisms that underlie systematic changes in 3′ UTR lengths remain to be characterized. Through a uniform analysis of a large number of 3′ end sequencing data sets, we have...
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