Searching journal content for articles similar to Lu et al. 20 (9): 1238.

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  1. ...showing the counts of orthologs derived from Ensembl Compara (see Methods). (E) Boxplot showing counts of paralogs. (F) Boxplot of mean quantitative gene expression data log2(FPKM + 1), sourced from 11,726 rice RNA-seq samples. (G) Boxplot of mean prediction score (pLDDT) from the corresponding AlphaFold2...
  2. ...and (optional) extra ORFs, and mapped RNA-seq file(s). Other omics data presented with single-nucleotide resolution (SNR) can be input and visualized in parallel or independently. To visualize DNA and/or amino acid sequences, users can optionally provide the corresponding sequence file. Output plots can...
  3. ...data to perform gene-level transcriptomic analysis, a maximal representation of transcriptomic complexity is beneficial to ensure that as many RNA-seq reads as possible are correctly assigned to their gene of origin. This would require that the annotation captures the maximal extent of the gene even...
  4. ...predictions and RNA sequencing (RNA-seq) evidence-supported gene model building. Gene annotation relied on an extensive variety of public RNA-seq data from various tissues to improve gene model accuracy. The RefSeq gene annotation reports for each species provide a full accounting of all methodology deployed...
  5. ...(A) sites of PAT-seq data were confirmed by previously collected rice EST data (often sequenced by low throughput and Sanger method). There are ∼70% of the intergenic PACs that are confirmed by EST. Second, single-nucleotide profiles of these intergenic PACs surrounding the poly(A) sites (Supplemental Fig...
  6. ...and used Cufflink (Roberts et al. 2011) to call the expression values (FPKM) of annotated rice genes and to detect differentially expressed genes. We obtained 40.1 M of RNA-seq reads from seedlings, and 89.2% of them were mapped to the rice (Tigr release 5). Similarly, we obtained 29.6million reads from...
  7. ..., comprehensive studies of transcriptomes at single base resolution are rare, even for modern organisms, and lacking for rice. Here, we present the first transcriptome atlas for eight organs of cultivated rice. Using high-throughput paired-end RNA-seq, we unambiguously detected transcripts expressing...
  8. ...) and therefore may play a fundamental role in the establishment of organismal complexity (Black 2003; Mudge et al. 2011; La Cognata et al. 2014). The -wide analysis of AS has been done primarily using exon microarrays first and, more recently, short-read RNA-seq. These two methods are effective...
  9. ...(Supplemental Fig. S11), suggesting that statistical power along with the resolution of RNA-seq is a contributor to finding eQTLs unique to this study. Genetic variants near each gene also affect alternative splicing; using isoform ratio (the fraction of a gene’s expression arising from each isoform) (Methods...
  10. .... Altogether, our results show that at least 61% of intron-containing genes are alternatively spliced under normal growth conditions, which indicates a high complexity of the Arabidopsis transcriptome. Results RNA-seq of a normalized cDNA library improves gene representation To facilitate the discovery...
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