Finds all intervals where track expression is 'TRUE'.
Usage
gscreen(
expr = NULL,
intervals = NULL,
iterator = NULL,
band = NULL,
intervals.set.out = NULL
)Arguments
- expr
logical track expression
- intervals
genomic scope for which the function is applied
- iterator
track expression iterator. If 'NULL' iterator is determined implicitly based on track expression.
- band
track expression band. If 'NULL' no band is used.
- intervals.set.out
intervals set name where the function result is optionally outputted
Details
This function finds all intervals where track expression's value is 'TRUE'.
If 'intervals.set.out' is not 'NULL' the result is saved as an intervals set. Use this parameter if the result size exceeds the limits of the physical memory.
NaN values
A track expression evaluates to NaN wherever the iterator produces a bin
the track has no data for. What happens next depends on the function:
gextractkeepsNaNrows, so the result has one row per iterator interval whether or not the track covered it.gsummarycounts them and reports the count as the "NaN intervals" element, while the statistics themselves are computed over the non-NaNvalues only.gdist,gquantilesandgscreendrop them:NaNbins are not counted into any distribution bin, do not contribute to a percentile, and never satisfy a screening condition - including a condition that would be true of every real value.gsegmentspans them: aNaNbin contributes no evidence to the test that places a boundary, but it still falls inside whichever segment surrounds it, so the returned segments tile the scope continuously rather than skipping the gaps.
So on 20 bins of which 7 are NaN, gextract returns 20 rows,
gsummary reports 20 total and 7 NaN, and gdist counts 13; and on a
300 kb scope where 120 of 300 bins are NaN, gsegment still returns
segments covering the full 300 kb.
The practical consequence is that NaN and zero are different, and
collapsing them with ifelse(is.na(x), 0, x) turns "no data here" into a
measured value of zero. Where that is genuinely what you want, note that it
also changes every mean, quantile and distribution computed downstream.
Examples
gdb.init_examples()
gscreen("dense_track > 0.2 & sparse_track < 0.4",
iterator = "dense_track"
)
#> chrom start end
#> 1 chr1 34850 34950
#> 2 chr1 47500 47550
#> 3 chr1 65100 65200
#> 4 chr1 65850 65950
#> 5 chr1 66050 66100
#> 6 chr1 92650 92700
#> 7 chr1 95350 95400
#> 8 chr1 100650 100700
#> 9 chr1 139050 139100
#> 10 chr1 152600 152650
#> 11 chr1 245500 245550
#> 12 chr1 341100 341150
#> 13 chr1 371450 371500
#> 14 chr1 373000 373100
#> 15 chr1 383550 383600
#> 16 chr1 459400 459450
#> 17 chr2 19200 19250
#> 18 chr2 22100 22150
#> 19 chr2 34250 34300
#> 20 chr2 34500 34550
#> 21 chr2 37400 37450
#> 22 chr2 50700 50750
#> 23 chr2 64050 64100
#> 24 chr2 69200 69250
#> 25 chr2 83550 83600
#> 26 chr2 100800 100850
#> 27 chr2 101450 101500
#> 28 chr2 139600 139650
#> 29 chr2 168600 168650
#> 30 chr2 233050 233100
#> 31 chr2 245200 245250
#> 32 chr2 282300 282350
#> 33 chrX 85150 85200