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  • eoh001
    Member
    • Mar 2011
    • 19

    #1

    Tophat with 454 reads

    Hello
    I was trying to find structural variations from 454 reads using tophat.
    However, all the results from tophat were empty.
    There seemed to be no problem with running tophat.
    I found that most of the 454 reads contained a long 5'-most extra sequence (39bp).

    5' tcag+ACGAGTGCGT+AAGCAGTGGTATCAACGCAGAGTT+ mRNA........3'
    ---- ------------- -------------------------------
    key MID cDNA library primer


    I wonder whether tophat trim the extra sequence off during alignment. Or should I remove them manually before I run tophat?

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