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  • doublealice
    Member
    • Feb 2011
    • 24

    RNA-seq reads counting matrix

    I have a list of reference genome loci coordinates. The short RNA reads were mapped on these loci by bowtie and samtools.

    Instead of simply get the counting number of reads, I hope to generate a matrix like this:
    Code:
    read-id   Loci1     Loci2     Loci3 .....
      1          2            4         0
      2          0            3         4
      3          4            2         5
    ...
    This is just an example showing that read1 aligned two different places in Loci1, 4 different places in loci2, none in loci3.

    I had made loci table in a gff format file and loaded it into R. All reads and alignment information is in bam file.

    I tried two ways to load bam file into R. One is:

    Code:
    reads<-readBamGappedAlignments("myalign_reads.sorted.bam")
    I found the output ignore my reads ID. Only chromosome and positions and other information are available. I need reads ID to count how many different places a read hits within one loci. This seems to be a limitation of the package.

    I also tried another method:
    Code:
    indexBam("myalign_reads.sorted.bam"0
    param<-ScanBamParam()
    reads<-scanBam("myalign_reads.sorted.bam", index="myalign_reads.sorted.bam", param=param)
    This loaded everything and read id was stored in qname. However, I don't know how to perform the further counting to generate the matrix.

    Can you give me any suggestion or idea on how to work on it? I tried my best but due to limit knowledge on R and bioconductor, I have suffered from it for several days.

    I appreciate if anyone can give me some hints or help me work it out. Thanks!

    Alice
  • areyes
    Senior Member
    • Aug 2010
    • 165

    #2
    Sorry, I did not watch your matrix correctly!
    Last edited by areyes; 04-19-2011, 04:03 AM. Reason: mistake

    Comment

    • doublealice
      Member
      • Feb 2011
      • 24

      #3
      I got some progress on this according to the manual from http://manuals.bioinformatics.ucr.edu/home/ht-seq
      on section "Computing Absolute and Relative Overlaps Among Ranges".

      Now, I have a list like this:
      Code:
      readid     loci-id
      1           105
      1            108
      3            114
      3            114
      2            120
      4            123
      3            123
      5            124
      5            125
      5            125
      6            128
      7            128
      6            128
      6            128
      8            128
      ...
      The next work is transform this table into my expected matrix, like:
      Code:
      readid   105 108  114  120  123  124  125  128
      1          1    1
      2                          1
      3                    2             1
      4                                       1
      5                                               1      2
      6                                                        3
      7                                                    1
      8                                                   1
      I don't know how to adjust the table to present it very well here. Anyway, it just shows how many different places a read mapped in a loci.

      To get this matrix also not easy for me. If you know any R function can work on it, please hint. Thank you very much!

      Alice

      =========
      I got it. Using table() can get that matrix.
      Last edited by doublealice; 04-19-2011, 01:04 PM.

      Comment

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