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  1. Genome-wide quantification of ADAR adenosine-to-inosine RNA …

    • For any set of predetermined genomic regions, the editing index is defined (Fig. 1a,b) as the ratio of the number of A-to-G mismatches (mismatches between RNA-seq reads aligned to the regions of interest and t… 展开

    Robustness of The Editing Index

    The purpose of the AEI is to allow a quantitative comparison of various RNA-seq samples, … 展开

    Nature
    Comparison with Alternative Approaches

    RNA edits can be systematically and directly observed in RNA-sequencing data, as inosines appear in the sequencing data as guanosines. Various algorithmic approaches and … 展开

    Nature
    Alu Editing in Various Tissues and Conditions

    We now turn to demonstrate how the AEI can be used to chart the editome across various conditions and tissues. First, we calculate the AEI for 8,848 GTEx samples, of 47 different tis… 展开

    Nature
     
  1. a2iEditing/RNAEditingIndexer - GitHub

  2. Calculate the Adenosine Editing Index (AEI) in single cells

  3. Divergent landscapes of A-to-I editing in postmortem and

  4. QEdit: RNA editing quantification in deep …

    The Alu editing index (AEI) is a metric to quantify the global RNA editing activity of sample and is defined as the weighted average of editing events occurring in all Alu elements. The pipeline to calculate AEI is described in Roth et al. …

  5. Genome-wide quantification of ADAR adenosine-to-inosine RNA …

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  7. 新工具可定量分析RNA碱基编辑器活性 - 科学网

  8. Spatial Visualization of A-to-I Editing in Cells Using …

    2024年7月7日 · A-to-I editing is the most widespread post-transcriptional modification and is essential for multiple biological processes. One way that editing impacts cellular pathways is thought to be through directing the …

  9. Calculate the Adenosine Editing Index (AEI) — calc_AEI

  10. Quantifying RNA Editing in Deep Transcriptome Datasets

    2020年3月5日 · Identification of differential RNA editing is most relevant at recoding sites, where altered A-to-I levels could lead to different protein isoforms. Editing dysregulation at recoding sites between two groups of samples is often …