All functions |
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Pre-calculated CpG distribution values for BSgenomes |
2019 ENCODE list of poorly mapped regions in hg38 |
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FANTOM5 regions for GRCh38 |
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Add coverage to a qseaSet using proper pairs and/or high-quality R1 reads |
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Add per-sample CNV calls to a qseaSet using HMMcopy |
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Summarise the fraction of hyper-stable methylated regions (GRCh38 only) |
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Add library metrics to the qseaSet sample table |
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Add MEDIPS-style enrichment metrics to a qseaSet sample table |
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Add qsea normalisation steps with defaults |
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Append window summaries to the sample table |
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Subset a qseaSet by overlaps / non-overlaps with genomic regions |
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Annotate genomic windows using ChIPseeker (with optional CpG/FANTOM context) |
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Arrange (reorder) samples in a qseaSet via dplyr syntax |
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Coerce common tabular inputs to GRanges |
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CpG enrichment from a BAM file (MEDIPS-style) |
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CpG enrichment from GRanges of reads (MEDIPS-style) |
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Fit GLM and return DMR data in one step |
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Fraction of thresholded windows overlapping a set of regions |
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Genome-wide CpG statistics (relH and GoGe) |
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Column names of a qseaSet sample table |
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Combine two qseaSets |
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Combine multiple qseaSets |
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Convert qsea beta values to array-like probe matrix |
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Count windows above a cutoff |
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Accessors for dimensionality reduction results |
Downsample reads in a qseaSet |
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A small example qseaSet with 5 paired tumour/normal samples. |
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A small example qseaSet with 5 paired tumour/normal samples. |
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Filter samples in a qseaSet |
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Filter regions (windows) inside a qseaSet |
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Fit a generalized linear model (GLM) to a qseaSet |
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GC content across the human genome (hg38/GRCh38) |
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Get beta per window |
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Genomic positions of a motif (CG) |
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Get counts per window |
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Extract DMR-level results from a fitted GLM |
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Extract per-window data (counts / NRPM / beta) |
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Generate a PCA from a qseaSet |
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Summarise signal by genomic context |
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Get annotation DB for current or specified genome |
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Get current mesa genome setting |
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Get TxDb for current or specified genome |
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Get NRPM per window |
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Infer pattern names from region density columns |
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Summarise key QC fields per sample |
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Get window names from a qseaSet, ranges/table or dimensionality reduction object |
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Extract the regions (windows) used in a qseaSet |
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hg19tohg38 liftover chain |
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CpG islands for hg38. |
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Ultra-stable methylated regions (GRCh38) |
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Infinium 450k probe locations for hg38. |
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Check whether an object is a qseaSet |
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Left-join onto the sample table of a mesaDimRed |
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Left join data onto a qseaSet sample table |
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Lift over genomic ranges from hg19 to hg38 |
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Generate all possible pairwise contrasts |
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Construct an initial qseaSet from BAMs and metadata |
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Make a wide sample-by-window table |
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Mappability across the human genome (hg38/GRCh38) |
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mesa: Methylation Enrichment Sequencing Analysis |
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Dimensionality reduction results container |
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PCA results container |
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UMAP results container |
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Mix two samples to generate a synthetic qseaSet sample |
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Mutate the sample table of a mesaDimRed |
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Mutate columns in a qseaSet sample table |
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Transform DMR results to long format |
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CNV heatmap across samples |
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Sample correlation heatmap |
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UpSet plot of DMR overlaps |
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Plot dimensionality reduction results |
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Plot sample signal over windows spanning a gene (± flanks) as a heatmap using ComplexHeatmap. The gene can be given as a HGNC symbol or Ensembl ID. |
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Distribution of windows across genomic features |
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Plot principal component analysis (PCA) results |
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Heatmap of signal across selected genomic regions |
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Plot UMAP results |
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Pool (merge) samples that share a common name prefix |
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Pull a column from a qseaSet sample table |
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Convert a makeTable-like data frame to GRanges (UCSC style) |
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Remove (zero out) CNV data from a qseaSet |
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Set library factors to 1 |
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Remove normalisation suffix from column names |
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Rename samples in a qseaSet by regex |
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Rename samples using a column from the sample table |
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Run HMMcopy on per-window reads for a single sample |
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Select or rename columns in a qseaSet sample table |
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Select or rename columns of a qseaSet sample table |
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Set or get an Ensembl/BioMart handle on a qseaSet |
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Set default OrgDb (annoDb) for downstream annotation helpers |
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Set default genome for downstream annotation helpers |
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Manage mesa parallelisation (set & query) |
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Set default TxDb for downstream annotation helpers |
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Take the top most DMRs per contrast, based on those with the largest value of the selected metric |
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Sort samples in a qseaSet |
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Subset a qseaSet by samples |
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Subset windows in a qseaSet by signal across samples |
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Subset windows above Poisson background |
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Summarise across windows per sample |
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Summarise DMRs by contrast |
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Summarise DMRs by gene |
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Write bigWig tracks per sample or group |
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Write DMR results to BED files |
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Write DMR results to an Excel workbook |
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