All functions |
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Get overlap between datatable of SNPs and scATAC peaks |
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Get overlap between data table of SNPs and HiChIP_FitHiChIP coaccessibility anchors |
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Plot CS bin counts |
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Bar plot of tool-specific CS sizes |
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IMPACT files |
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Query IMPACT annotations |
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Run motifbreakR |
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Calculate motifbreakR p-values |
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Merge and filter motifbreakR + echolocatoR results |
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Plot motifbreakR results |
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Summarize motifbreakR + echolocatoR results |
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Metadata and links to data |
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Plot brain cell-specific epigenomic data |
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Download cell type-specific epigenomic peaks |
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Import cell type-specific interactomes |
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Get cell type-specific promoter/emhancer/interactome data |
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Get regulatory regions: Nott2019 |
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Plot brain cell-specific interactome data |
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Gather Roadmap annotation metadata |
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Query Roadmap Query Roadmap annotations using a set of genomic coordinates. |
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XGR enrichment |
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XGR enrichment (bootstrapped) |
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Filter assays |
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Filter sources |
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Add Mb |
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Annotate any missense variants |
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Annotate merged fine-mapping results from all loci |
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Annotation file name |
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Convert plots to various formats |
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bulkATACseq peaks from human brain tissue |
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Cicero_coaccessibility from human brain tissue |
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FitHiChIP loop calls from human brain tissue |
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scATACseq cell type-specific peaks from human brain tissue |
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scATACseq peaks from human brain tissue |
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Brain cell type-specific interactomes with superenhancers |
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Get widow limits |
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Find GenomicRanges overlap Find overlap genomic position overlap between two GRanges objects. |
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Import bigwig files from the UCSC Genome Browser |
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Merge all cell-type-specific epigenomics |
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Plot inter-study SNP overlap |
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Plot any missense variants |
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Merge all summary plots into one super plot |
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Test enrichment |
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Example XGR query |
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Download, standardize, and merge XGR annotations |