Given a single row from an enrichment table calculation, finds the set of overlaps between the user set and the test set. You can then use these, for example, to get sequences for those regions.
extractEnrichmentOverlaps(locResult, userSets, regionDB)
locResult | Results from runLOLA function |
---|---|
userSets | User sets passed to the runLOLA function |
regionDB | Region database used |
userSets overlapping the supplied database entry.
#>#>#>#>#>#>data("sample_universe", package="LOLA") data("sample_input", package="LOLA") getRegionSet(regionDB, collections="ucsc_example", filenames="vistaEnhancers.bed")#> GRangesList object of length 1: #> [[1]] #> GRanges object with 1339 ranges and 0 metadata columns: #> seqnames ranges strand #> <Rle> <IRanges> <Rle> #> 1 chr1 [ 3190582, 3191428] * #> 2 chr1 [ 8130440, 8131887] * #> 3 chr1 [10593124, 10594209] * #> 4 chr1 [10732071, 10733118] * #> 5 chr1 [10757665, 10758631] * #> ... ... ... ... #> 1335 chrX [139380917, 139382199] * #> 1336 chrX [139593503, 139594774] * #> 1337 chrX [139674500, 139675403] * #> 1338 chrX [147829017, 147830159] * #> 1339 chrX [150407693, 150409052] * #> #> ------- #> seqinfo: 69 sequences from an unspecified genome; no seqlengths#>#>#>#>#>#>#> GRangesList object of length 1: #> [[1]] #> GRanges object with 1339 ranges and 0 metadata columns: #> seqnames ranges strand #> <Rle> <IRanges> <Rle> #> 1 chr1 [ 3190582, 3191428] * #> 2 chr1 [ 8130440, 8131887] * #> 3 chr1 [10593124, 10594209] * #> 4 chr1 [10732071, 10733118] * #> 5 chr1 [10757665, 10758631] * #> ... ... ... ... #> 1335 chrX [139380917, 139382199] * #> 1336 chrX [139593503, 139594774] * #> 1337 chrX [139674500, 139675403] * #> 1338 chrX [147829017, 147830159] * #> 1339 chrX [150407693, 150409052] * #> #> ------- #> seqinfo: 23 sequences from an unspecified genome; no seqlengths#>#>#>#>#> [1] "/sfs/lustre/scratch/ns5bc/code/LOLA/inst/extdata/hg19/ucsc_example/regions/vistaEnhancers.bed"#>#>#>locResult = res[2,] extractEnrichmentOverlaps(locResult, userSets, regionDB)#> GRanges object with 632 ranges and 0 metadata columns: #> seqnames ranges strand #> <Rle> <IRanges> <Rle> #> [1] chr1 [18229570, 19207602] * #> [2] chr1 [35350878, 35351854] * #> [3] chr1 [38065507, 38258622] * #> [4] chr1 [38499473, 39306315] * #> [5] chr1 [42611485, 42611691] * #> ... ... ... ... #> [628] chrX [125299245, 125300436] * #> [629] chrX [136032577, 138821238] * #> [630] chrX [139018365, 148549454] * #> [631] chrX [154066672, 154251301] * #> [632] chrY [ 2880166, 7112793] * #> ------- #> seqinfo: 69 sequences from an unspecified genome; no seqlengths#>userSetsRedefined = redefineUserSets(userSets, userUniverse) resRedefined = runLOLA(userSetsRedefined, userUniverse, regionDB, cores=1)#>#>#>