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
    Current Approaches to Protein Sequencing
    by seqadmin


    Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
    04-04-2024, 04:25 PM
  • seqadmin
    Strategies for Sequencing Challenging Samples
    by seqadmin


    Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
    03-22-2024, 06:39 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by seqadmin, 04-11-2024, 12:08 PM
0 responses
30 views
0 likes
Last Post seqadmin  
Started by seqadmin, 04-10-2024, 10:19 PM
0 responses
32 views
0 likes
Last Post seqadmin  
Started by seqadmin, 04-10-2024, 09:21 AM
0 responses
28 views
0 likes
Last Post seqadmin  
Started by seqadmin, 04-04-2024, 09:00 AM
0 responses
52 views
0 likes
Last Post seqadmin  
Working...
X