All functions |
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Run the derfinder analysis on a chromosome |
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Assign genomic states to regions |
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Calculate p-values and identify regions |
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Calculate F-statistics at base pair resolution from a loaded BAM files |
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Coerce the coverage to a GRanges object for a given sample |
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Collapse full coverage information for efficient quantile computations |
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Extract coverage information for exons |
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Export coverage to BigWig files |
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Create a BigWig file with the coverage information for a given sample |
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Define a cluster to use. |
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Deprecated functions in package ‘derfinder’ |
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Change naming style for a set of sequence names |
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Filter the positions of interest |
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Find non-zero regions in a Rle |
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Load the unfiltered coverage information from a group of BAM files and a list of chromosomes |
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Genome samples processed data |
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Genome samples processed data |
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F-statistics for the example data |
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Genome samples information |
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Candidate DERs for example data |
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Genomic State for Hsapiens.UCSC.hg19.knownGene |
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Extract coverage information for a set of regions |
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Calculate the total number of mapped reads |
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Load the coverage information from a group of BAM files |
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Obtain the genomic state per region from annotation |
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Build model matrices for differential expression |
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Merge results from different chromosomes |
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Transform and split the data |
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Identify regions data by a coverage filter and get a count matrix from BigWig files |
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Construct full paths to a group of raw input files |
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Identify regions data by a coverage filter and get a count matrix |
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Calculate adjustments for library size |