Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • SOLiD WTP alignment file: representation of spliced reads

    Hi

    I've got a data set with SOLiD RNA-Seq data that was aligned with SOLiD's whole transcriptome analysis pipeline (WTP 1.2.1). This software produces a GFF file that represents each read with one line, or, if the read straddles a splice junction, wth two lines (which are usually not next to each other).

    I have trouble understanding how the spliced reads are represented.

    Here is a normal read:
    Code:
    chr2L   wtp     read    75079   75113   30      +       .       bd=1445_1152_746_F3;rs=16;mm=0;g=T12003120303000210002013210322101003330110312122223;i=1;
    There are 0 mismatches (mm=0) and 16 bases skipped (rs=16). if I convert the read to sequence space and extract the part at the indicated coordinates from my refernce FASTA, this alignes nicely:

    Code:
    TGAAATGAATTAAAAGTTTTCCATCAATCTGGTTTATAACAATGACTCTCG  [read]
                    TTTTCCATCAATCTGGTTTATAACAATGACTCTCG  [reference, 2L:75079-75113]
    ----------------  [ <-- 16 skipped]
    Now for a spliced read. This bead ID here appears twice:

    Code:
    chr2L   wtp     read    108217  108226  45      +       .       bd=1636_459_310_F3;rs=1;mm=0;g=T32012102331321332201132130130000113020000230013032;i=1;jp=108588;jt=k;
    chr2L   wtp     read    108588  108622  45      +       .       bd=1636_459_310_F3;rs=1;mm=0;g=T32012102331321332201132130130000113020000230013032;i=1;jp=108217;jt=k;
    The two lines refer each others starting positions via the 'jp' attribute. However if I extract the indicates positions, there is no match:

    Code:
    TAGGTCAAGCGTAGTATCTTGTAGTAACGGGGGTGCCTTTTTCGGGTAATC   [read]
     CTCAGAATCA                                           [reference, 2L:108217-108226]
               CTCCACCAACAATTTAGCCGACCGGAACTCGGGTT        [reference, 2L:108588-108622]
    I can't find these reference parts anywhere in the read.

    I tried many different reads, and always, the non-spliced ones agree with the reference (unless there are mismatches, causing the colour space decoding to lose sync) and the spliced ones don't. Do I have to do something different if I decode colour space for a spliced read? Do I misunderstand the WTP output format? Or is something going severely wrong here?

    Thanks for any hints

    Simon
    Last edited by Simon Anders; 08-23-2010, 02:55 AM. Reason: corrected GFF excerpt

Latest Articles

Collapse

  • seqadmin
    Recent Advances in Sequencing Analysis Tools
    by seqadmin


    The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
    05-06-2024, 07:48 AM
  • seqadmin
    Essential Discoveries and Tools in Epitranscriptomics
    by seqadmin




    The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
    04-22-2024, 07:01 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by seqadmin, 05-10-2024, 06:35 AM
0 responses
20 views
0 likes
Last Post seqadmin  
Started by seqadmin, 05-09-2024, 02:46 PM
0 responses
26 views
0 likes
Last Post seqadmin  
Started by seqadmin, 05-07-2024, 06:57 AM
0 responses
21 views
0 likes
Last Post seqadmin  
Started by seqadmin, 05-06-2024, 07:17 AM
0 responses
21 views
0 likes
Last Post seqadmin  
Working...
X