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