Hi Malcolm,

The requirement that names of a GRangesList must be unique has actually
been dropped in BioC 2.9 (current devel):

  > library(GenomicRanges)
  > grl <- GRangesList(a=GRanges(), a=GRanges())
  > validObject(grl)
  [1] TRUE

Note that before BioC 2.9 this requirement was not only for GRangesList
but also for GRanges objects. In BioC 2.9, this requirement has been
dropped for both containers:

  > gr <- GRanges(c("chr1", "chr1"), IRanges(1:2, 4:5, names=c("a", "a")))
  > validObject(gr)
  [1] TRUE

Cheers,
H.

> sessionInfo()
R Under development (unstable) (2011-07-31 r56578)
Platform: x86_64-unknown-linux-gnu (64-bit)

locale:
 [1] LC_CTYPE=en_CA.UTF-8       LC_NUMERIC=C
 [3] LC_TIME=en_CA.UTF-8        LC_COLLATE=en_CA.UTF-8
 [5] LC_MONETARY=en_CA.UTF-8    LC_MESSAGES=en_CA.UTF-8
 [7] LC_PAPER=C                 LC_NAME=C
 [9] LC_ADDRESS=C               LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_CA.UTF-8 LC_IDENTIFICATION=C

attached base packages:
[1] stats     graphics  grDevices utils     datasets  methods   base

other attached packages:
[1] GenomicFeatures_1.5.16 GenomicRanges_1.5.21   IRanges_1.11.17

loaded via a namespace (and not attached):
 [1] Biobase_2.13.7      biomaRt_2.9.2       Biostrings_2.21.7
 [4] BSgenome_1.21.3     DBI_0.2-5           RCurl_1.6-6
 [7] RSQLite_0.9-4       rtracklayer_1.13.10 XML_3.4-0
[10] zlibbioc_0.1.7


On 11-08-03 09:23 AM, Cook, Malcolm wrote:
Hi,

re: https://stat.ethz.ch/pipermail/bioc-sig-sequencing/2011-February/001867.html

It appears that the requirement that names of a GRangesList must be unique has 
won the day.

I'm not sure I agree with this result, as there are many operations that are 
optimized for GRangesList that have use cases that do not depend upon such 
uniqueness.

However, I find that such operations can proceed after setting the names to 
NULL,, as is demonstrated in the R session following my signature, in which I 
am creating a GRanges list with entirely duplicate (unnamed) elements.

I hope this workaround proves useful to others...

Malcolm Cook
Computational Biology - Stowers Institute for Medical Research



Example:

grl=GRangesList(a=GRanges(c(10,20,30),c(15,25,35)),b=GRanges(c(100,200,300),c(150,250,350)))
grl
GRangesList of length 2
$a
GRanges with 3 ranges and 0 elementMetadata values
     seqnames    ranges strand |
        <Rle>  <IRanges>   <Rle>  |
[1]       10  [15, 15]      * |
[2]       20  [25, 25]      * |
[3]       30  [35, 35]      * |

$b
GRanges with 3 ranges and 0 elementMetadata values
     seqnames     ranges strand |
        <Rle>   <IRanges>   <Rle>  |
[1]      100 [150, 150]      * |
[2]      200 [250, 250]      * |
[3]      300 [350, 350]      * |


seqlengths
   10  20  30 100 200 300
   NA  NA  NA  NA  NA  NA
grl[rep(1,2)]
Error in `rownames<-`(`*tmp*`, value = c("a", "a")) :
   duplicate rownames not allowed
names(grl)=NULL
grl[rep(1,2)]
GRangesList of length 2
[[1]]
GRanges with 3 ranges and 0 elementMetadata values
     seqnames    ranges strand |
        <Rle>  <IRanges>   <Rle>  |
[1]       10  [15, 15]      * |
[2]       20  [25, 25]      * |
[3]       30  [35, 35]      * |

[[2]]
GRanges with 3 ranges and 0 elementMetadata values
     seqnames    ranges strand |
        <Rle>  <IRanges>   <Rle>  |
[1]       10  [15, 15]      * |
[2]       20  [25, 25]      * |
[3]       30  [35, 35]      * |


seqlengths
   10  20  30 100 200 300
   NA  NA  NA  NA  NA  NA


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--
Hervé Pagès

Program in Computational Biology
Division of Public Health Sciences
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