From a GRanges object to a GRangeList
1
1
Entering edit mode
@patrick-schorderet-6081
Last seen 9.6 years ago
United States

Hi All,

I'm trying to create a GRangesList from a GRanges object. I basically have a Granges object called miRNA. It has 302 ranges. I also have a function that requires me to feed it with a GrangesList, so I am trying to alter the Granges object to a list format with each element of the list containing a single range I am sure there is an easy way to do this, but I can't wrap my head around it.

Thanks for any help.

 

> miRNA
GRanges object with 304 ranges and 3 metadata columns:
        seqnames               ranges strand   |     tx_name         gene_id     tx_type
           <Rle>            <IRanges>  <Rle>   | <character> <CharacterList> <character>
    [1]       2L   [ 857596,  857617]      +   | FBtr0304183     FBgn0262177       miRNA
    [2]       2L   [2737568, 2737589]      +   | FBtr0309710     FBgn0263564       miRNA
    [3]       2L   [3767667, 3767688]      +   | FBtr0304276     FBgn0262392       miRNA
    [4]       2L   [4343736, 4343756]      +   | FBtr0304206     FBgn0262375       miRNA
    [5]       2L   [5068596, 5068617]      +   | FBtr0304262     FBgn0262213       miRNA
    ...      ...                  ...    ... ...         ...             ...         ...
  [300]        X [16191270, 16191291]      -   | FBtr0304409     FBgn0262283       miRNA
  [301]        X [19169201, 19169222]      -   | FBtr0309726     FBgn0263571       miRNA
  [302]        X [21296386, 21296407]      -   | FBtr0304484     FBgn0262454       miRNA
  [303]        X [21298279, 21298300]      -   | FBtr0309696     FBgn0263559       miRNA
  [304]        X [22833545, 22833566]      -   | FBtr0304314     FBgn0262237       miRNA
  -------
  seqinfo: 1870 sequences from an unspecified genome

 

 

 

 

 

 

granges grangeslist • 2.4k views
ADD COMMENT
1
Entering edit mode
@james-w-macdonald-5106
Last seen 17 hours ago
United States

It's as obvious as you might think:

> mirnas <- microRNAs(TxDb.Hsapiens.UCSC.hg19.knownGene)
Loading required package: mirbase.db
> mirnas
GRanges object with 1595 ranges and 1 metadata column:
         seqnames                 ranges strand   |       mirna_id
            <Rle>              <IRanges>  <Rle>   |    <character>
     [1]     chr1     [  30366,   30503]      +   | hsa-mir-1302-2
     [2]     chr1     [ 567705,  567793]      -   |   hsa-mir-6723
     [3]     chr1     [1102484, 1102578]      +   |   hsa-mir-200b
     [4]     chr1     [1103243, 1103332]      +   |   hsa-mir-200a
     [5]     chr1     [1104385, 1104467]      +   |    hsa-mir-429
     ...      ...                    ...    ... ...            ...
  [1591]     chrX [154115635, 154115733]      -   | hsa-mir-1184-1
  [1592]     chrX [154612749, 154612847]      -   | hsa-mir-1184-2
  [1593]     chrX [154687178, 154687276]      +   | hsa-mir-1184-3
  [1594]     chrY [  1362811,   1362885]      +   | hsa-mir-3690-2
  [1595]     chrY [  2477232,   2477295]      +   | hsa-mir-6089-2
  -------
  seqinfo: 93 sequences (1 circular) from hg19 genome
> as(mirnas, "GRangesList")
GRangesList object of length 1595:
[[1]]
GRanges object with 1 range and 1 metadata column:
      seqnames         ranges strand |       mirna_id
         <Rle>      <IRanges>  <Rle> |    <character>
  [1]     chr1 [30366, 30503]      + | hsa-mir-1302-2

[[2]]
GRanges object with 1 range and 1 metadata column:
      seqnames           ranges strand |     mirna_id
  [1]     chr1 [567705, 567793]      - | hsa-mir-6723

[[3]]
GRanges object with 1 range and 1 metadata column:
      seqnames             ranges strand |     mirna_id
  [1]     chr1 [1102484, 1102578]      + | hsa-mir-200b

...
<1592 more elements>
-------
seqinfo: 93 sequences (1 circular) from hg19 genome
>
ADD COMMENT
0
Entering edit mode

Great, that's exactly what I was looking for.

Is there an easy way to use the mirna_id as names for the list elements? and do this in one go?

ADD REPLY
0
Entering edit mode
> mirs <- microRNAs(TxDb.Hsapiens.UCSC.hg19.knownGene)
> nam <- mcols(mirs)[,1]
> mirs <- as(mirs, "GRangesList")
> names(mirs) <- nam
> mirs
GRangesList object of length 1595:
$hsa-mir-1302-2
GRanges object with 1 range and 1 metadata column:
      seqnames         ranges strand |       mirna_id
         <Rle>      <IRanges>  <Rle> |    <character>
  [1]     chr1 [30366, 30503]      + | hsa-mir-1302-2

$hsa-mir-6723
GRanges object with 1 range and 1 metadata column:
      seqnames           ranges strand |     mirna_id
  [1]     chr1 [567705, 567793]      - | hsa-mir-6723

$hsa-mir-200b
GRanges object with 1 range and 1 metadata column:
      seqnames             ranges strand |     mirna_id
  [1]     chr1 [1102484, 1102578]      + | hsa-mir-200b

...
<1592 more elements>
-------
seqinfo: 93 sequences (1 circular) from hg19 genome
>

 

ADD REPLY
0
Entering edit mode

Two other solutions

grl1 = setNames(as(mirs, "GRangesList"), mirs$mirna_id)
split(mirs, mirs$mirna_id)
## also: splitAsList(mirs, mirs$mirna_id)

and for the first a sanity check

> identical(names(grl1), unlist(grl1)$mirna_id)
[1] TRUE

 

 

ADD REPLY
0
Entering edit mode

But please be aware that using split() doesn't give you the same result:

grl2 <- split(mirs, mirs$mirna_id)
> identical(grl1, grl2)
[1] FALSE

This is because the mirna_id metadata column contains some duplicates, which causes split() to generate some list elements with more than 1 range in them:

> table(elementLengths(grl2))
   1    2 
1593    1 

> grl2[elementLengths(grl2) != 1]
GRangesList object of length 1:
$hsa-mir-6511b-1 
GRanges object with 2 ranges and 1 metadata column:
      seqnames               ranges strand |        mirna_id
         <Rle>            <IRanges>  <Rle> |     <character>
  [1]    chr16 [ 2156670,  2156754]      - | hsa-mir-6511b-1
  [2]    chr16 [15227923, 15228007]      - | hsa-mir-6511b-1

-------
seqinfo: 93 sequences (1 circular) from hg19 genome

This might or might not be what you want.

H.

ADD REPLY

Login before adding your answer.

Traffic: 812 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6