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  • seb567
    Senior Member
    • Jul 2008
    • 260

    #1

    One read has many alignments starting at the same position

    Dear SEQanswers,

    I have a particular gene. I use its sequence as a reference to gather an atlas of variations induced by some enzyme, whose target is located within the said gene sequence.


    The sequence of the region of interest follows.


    Code:
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca
    In the sequence, two repeated 4-mers are colored in red.


    I also happen to have two short reads obtained by DNA sequencing.

    FORWARD:

    gatattgatattggtcttaatatgacttgttttcattgttctcagccagcatggcagcctctttcccacccac


    REVERSE:

    tggtcttaatatgacttgttttcattgttctcagccagcatggcagcctctttcccacccaccttgggactca


    Aligning these sequences onto the aforementioned reference sequence can potentially produce at least 5 alignments, regardless of utilized alignment software & algorithms.




    Alignment 1


    Code:
    gatattgatattggtcttaatatgacttgttttcattgttctca---------gccagcatggcagcctctttcccacccac FORWARD
               tggtcttaatatgacttgttttcattgttctca---------gccagcatggcagcctctttcccacccaccttgggactca REVERSE
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca GENE

    Alignment 2


    Code:
    gatattgatattggtcttaatatgacttgttttcattgttctc---------agccagcatggcagcctctttcccacccac FORWARD
               tggtcttaatatgacttgttttcattgttctc---------agccagcatggcagcctctttcccacccaccttgggactca REVERSE
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca GENE

    Alignment 3


    Code:
    gatattgatattggtcttaatatgacttgttttcattgttct---------cagccagcatggcagcctctttcccacccac FORWARD
               tggtcttaatatgacttgttttcattgttct---------cagccagcatggcagcctctttcccacccaccttgggactca REVERSE
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca GENE

    Alignment 4

    Code:
    gatattgatattggtcttaatatgacttgttttcattgttc---------tcagccagcatggcagcctctttcccacccac FORWARD
               tggtcttaatatgacttgttttcattgttc---------tcagccagcatggcagcctctttcccacccaccttgggactca REVERSE
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca GENE


    Alignment 5


    Code:
    gatattgatattggtcttaatatgacttgttttcattgtt---------ctcagccagcatggcagcctctttcccacccac FORWARD
               tggtcttaatatgacttgttttcattgtt---------ctcagccagcatggcagcctctttcccacccaccttgggactca REVERSE
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca GENE

    Alignment 6

    Code:
    gatattgatattggtcttaatatgacttgttttcattgt--t-------ctcagccagcatggcagcctctttcccacccac FORWARD
               tggtcttaatatgacttgttttcattgt--t-------ctcagccagcatggcagcctctttcccacccaccttgggactca REVERSE
    gatattgatattggtcttaatatgacttgttttcattgtt[COLOR="Red"]ctca[/COLOR]ggtac[COLOR="Red"]ctca[/COLOR]gccagcatggcagcctctttcccacccaccttgggactca GENE
    (alignments omitted)


    I can rule out the alignment number 6 and similar omitted alignments by considering them too complex in comparison to the 5 others.



    Therefore, there is a deletion of 9 nucleotides.

    However, the deletion can potentially start at 5 different positions.


    Based solely on sequence information, I think there is just nothing that can be done to retrieve the true starting position of the deletion.



    SEQanswers, what do you think ?

    -Seb
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    There is no "true" start. But there's probably a guideline as to whether one reports alignment 1 or 4. 4 puts the deletion as far left as possible, 1 puts it as far right as possible.

    I'm not sure that current SNP databases are currently consistent about this; I'm pretty sure I found a few places in the mouse genome where the same indel was reported under two ID's because of ambiguities like that.

    So if you don't know which way is preferred, pick one, and make note of which way you picked.

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