All functions | 
      |
|---|---|
BRGenomics: Tools for the Efficient Analysis of High-Resolution Genomics Data  | 
      |
PRO-seq data from Drosophila S2 cells  | 
      |
Apply normalization factors to GRanges object  | 
      |
Generating and Aggregating Data Within N-dimensional Bins  | 
      |
Bootstrapping Mean Signal by Position for Metaplotting  | 
      |
Extract Genebodies  | 
      |
Get signal counts at each position within regions of interest  | 
      |
Get signal counts in regions of interest  | 
      |
Get DESeqDataSet objects for downstream analysis  | 
      |
Get DESeq2 results using reduced dispersion matrices  | 
      |
Find sites with max signal in regions of interest  | 
      |
Calculate pausing indices from user-supplied promoters & genebodies  | 
      |
Filtering and counting spike-in reads  | 
      |
Calculating spike-in normalization factors  | 
      |
Get strand-specific coverage  | 
      |
Import basepair-resolution files  | 
      |
| 
           
  | 
        Import bam files  | 
      
Intersect or reduce ranges according to gene names  | 
      |
Constructing and checking for base-pair resolution GRanges objects  | 
      |
Merge GRanges objects  | 
      |
Merge replicates of basepair-resolution GRanges objects  | 
      |
Randomly subsample reads according to spike-in normalization  | 
      |
Randomly subsample reads from GRanges dataset  | 
      |
Subset regions of interest by quantiles of overlapping signal  | 
      |
Remove odd chromosomes from GRanges objects  | 
      |
Ensembl transcripts for Drosophila melanogaster, dm6, chromosome 4.  | 
      |