Searching journal content for articles similar to Park et al. 22 (9): 1626.

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  1. ...Multitissue single-nucleus RNA-seq reveals cell type–specific regulatory patterns of alternative polyadenylation in pigs Qiuhan Wen1,2, Zhen Wang1, Qi Bao1, Tianli Ding1, Haihan Zhang3, Jianbo Li4, Zhuang Liu5, Jieping Huang2 and Guoqiang Yi1,6,7 1Shenzhen Branch, Guangdong Laboratory of Lingnan...
  2. ...to construct RNA-seq libraries, and bodies were subjected to DNA resequencing. The reliable RNA–DNA differences (RDDs) were regarded as RNA editing sites. (B) The number of different types of mismatches in the RDDs. Only the RDDs in the genic region were considered. A-to-G RDDs represent A-to-I RNA editing...
  3. ...extrinsic and intrinsic evidence. Extrinsic evidence is extracted from transcripts and cross-species homologous proteins. RNA-seq reads offer direct evidence on introns and, if assembled, on a gene structure. Protein sequences from related s can be used to identify regions of a that encode proteins...
  4. ...editing.Accordingly, many tools have also been developed for the identification and quantification of APA based on RNA-seq data. Almost all of them are designed to detect the drops in RNA-seq read coverage along the gene body. However, due to high fluctuation of the sequencing coverage potentially caused...
  5. ...that these results can be generalized for other types of functional sequencing assays, we calculated mapping error rates for the H3K4me3 histone modification ChIP-seq data set from the ENCODE consortium (Supplemental Fig. S37). Similar to the RNA-seq results, the error rate for reads overlapping homozygous variants...
  6. ...upregulated following METTL2A knockdown (Fig. 4D). These upregulated m3C RNAs were enriched in mitochondrial-related genes (Supplemental Fig. S10A). These findings were further supported by the short-read RNA-seq results (Supplemental Fig. S10B–D). Furthermore, additional analyses demonstrated...
  7. ...PCR and high-throughput sequencing. No significant off-target effects were detected by this method (Supplemental Fig. S5). RNA-seq analysis of seven-gene-edited cells revealed increased expression of genes involved in DNA replication, repair pathways, p53 signaling, and cancer-related pathways...
  8. ...importance for further evaluating its biological significance. Here, we developed IPAFinder, a bioinformatic method for the de novo identification of intronic poly(A) sites and their dynamic changes from standard RNA-seq data. Applying IPAFinder to 256 pan-cancer tumor/normal pairs across six tumor types, we...
  9. ...peptides to the immune system (Voorter et al. 2016), it is critical to understand how polymorphisms impact HLA pre-mRNA maturation. However, due to the technical challenges associated with analyzing HLA transcripts using short-read RNA-seq reads, HLA genetic variation has been primarily studied at the DNA...
  10. ...to quantify transposable element (TE) RNA expression, such as RT-qPCR and RNA-seq, that do not distinguish between TEs expressed from their own promoter (bona fide) and TEs that are transcribed from a neighboring gene promoter such as within an intron or exon. This distinction is important owing...
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