[Bioc-sig-seq] Resizing a GRanges object with elements on the "*" strand
Ivan Gregoretti
ivangreg at gmail.com
Tue Sep 14 18:36:26 CEST 2010
Hello Leonardo,
I believe that the issue here is that resize() does not support the
"fix" argument at all when handling GRanges.
Actually that would be a nice upgrade of functionality for GRanges.
I face the same limitation and I currently resize by hand. :(
This is my work around:
library(GenomicRanges)
# a set of genomic features called C
C <- GRanges(seqnames=c("chr1","chr2","chr19","chrX"),
ranges=IRanges(start=c(0,0,5,1),
end=c(150,150,150,400)),
strand=c("*","-","*","+"),
score=c(10,20,30,90))
# peek at C
C
GRanges with 4 ranges and 1 elementMetadata value
seqnames ranges strand | score
<Rle> <IRanges> <Rle> | <numeric>
[1] chr1 [0, 150] * | 10
[2] chr2 [0, 150] - | 20
[3] chr19 [5, 150] * | 30
[4] chrX [1, 400] + | 90
seqlengths
chr1 chr19 chr2 chrX
NA NA NA NA
# this is the workaround
ranges(C) <- resize(ranges(C),1,fix="start")
# peek at the resized set C
C
GRanges with 4 ranges and 1 elementMetadata value
seqnames ranges strand | score
<Rle> <IRanges> <Rle> | <numeric>
[1] chr1 [0, 0] * | 10
[2] chr2 [0, 0] - | 20
[3] chr19 [5, 5] * | 30
[4] chrX [1, 1] + | 90
seqlengths
chr1 chr19 chr2 chrX
NA NA NA NA
Cheers,
Ivan
Ivan Gregoretti, PhD
National Institute of Diabetes and Digestive and Kidney Diseases
National Institutes of Health
5 Memorial Dr, Building 5, Room 205.
Bethesda, MD 20892. USA.
Phone: 1-301-496-1016 and 1-301-496-1592
Fax: 1-301-496-9878
On Tue, Sep 14, 2010 at 11:36 AM, Leonardo Collado Torres
<lcollado at ibt.unam.mx> wrote:
> Hello,
>
> I have a rather simple question that involves GenomicRanges' design.
>
> Basically, I have a GRanges object where all the elements are from the
> undefined "*" strand. I just want to resize them to get the 1st (from left
> to right) base. However, I'm not able to do so with the "resize" function
> even when specifying fix = "start" as it uses the fix = "center" method. Is
> this the desired performance? I have 2 workarounds, but I'm puzzled as the
> "flank" function actually uses the start (left to right) when elements are
> from the "*" strand. Is there a quicker way to do this or should I stick to
> the flank + shift workaround?
>
> Thank you and greetings,
> Leonardo
>
>> testGR <- GRanges( seqnames = rep("test", 3), ranges = IRanges ( start =
> c(10,100,1000), width = c(10, 100, 1000)), strand = Rle(strand(c("+","-")),
> c(1,2)) )
>> testGR
> GRanges with 3 ranges and 0 elementMetadata values
> seqnames ranges strand |
> <Rle> <IRanges> <Rle> |
> [1] test [ 10, 19] + |
> [2] test [ 100, 199] - |
> [3] test [1000, 1999] - |
>
> seqlengths
> test
> NA
>> resize(testGR, 1, fix="start")
> GRanges with 3 ranges and 0 elementMetadata values
> seqnames ranges strand |
> <Rle> <IRanges> <Rle> |
> [1] test [ 10, 10] + |
> [2] test [ 199, 199] - |
> [3] test [1999, 1999] - |
>
> seqlengths
> test
> NA
>> testGR2 <- GRanges( seqnames = rep("test", 3), ranges = IRanges ( start =
> c(10,100,1000), width = c(10, 100, 1000)), strand = Rle(strand(c("*")),
> c(3)) )
>> testGR2
> GRanges with 3 ranges and 0 elementMetadata values
> seqnames ranges strand |
> <Rle> <IRanges> <Rle> |
> [1] test [ 10, 19] * |
> [2] test [ 100, 199] * |
> [3] test [1000, 1999] * |
>
> seqlengths
> test
> NA
>> resize(testGR2, 1, fix="start")
> GRanges with 3 ranges and 0 elementMetadata values
> seqnames ranges strand |
> <Rle> <IRanges> <Rle> |
> [1] test [ 14, 14] * |
> [2] test [ 149, 149] * |
> [3] test [1499, 1499] * |
>
> seqlengths
> test
> NA
>
>> testGR3 <- GRanges ( seqnames = seqnames(testGR2), ranges = IRanges( start
> = start(testGR2), width = 1), strand = strand(testGR2) )
>>
>> testGR3
> GRanges with 3 ranges and 0 elementMetadata values
> seqnames ranges strand |
> <Rle> <IRanges> <Rle> |
> [1] test [ 10, 10] * |
> [2] test [ 100, 100] * |
> [3] test [1000, 1000] * |
>
> seqlengths
> test
> NA
>>
>
>> testGR4 <- shift(flank( testGR2, 1), 1)
>> testGR4
> GRanges with 3 ranges and 0 elementMetadata values
> seqnames ranges strand |
> <Rle> <IRanges> <Rle> |
> [1] test [ 10, 10] * |
> [2] test [ 100, 100] * |
> [3] test [1000, 1000] * |
>
> seqlengths
> test
> NA
>
>> sessionInfo()
> R version 2.12.0 Under development (unstable) (2010-09-08 r52880)
> Platform: x86_64-unknown-linux-gnu (64-bit)
>
> locale:
> [1] LC_CTYPE=en_US.utf8 LC_NUMERIC=C
> [3] LC_TIME=en_US.utf8 LC_COLLATE=en_US.utf8
> [5] LC_MONETARY=C LC_MESSAGES=en_US.utf8
> [7] LC_PAPER=en_US.utf8 LC_NAME=C
> [9] LC_ADDRESS=C LC_TELEPHONE=C
> [11] LC_MEASUREMENT=en_US.utf8 LC_IDENTIFICATION=C
>
> attached base packages:
> [1] stats graphics grDevices utils datasets methods base
>
> other attached packages:
> [1] GenomicRanges_1.1.25 IRanges_1.7.33
>
> loaded via a namespace (and not attached):
> [1] tools_2.12.0
>
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>
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