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  • nozzer
    Junior Member
    • Apr 2010
    • 2

    #1

    constructing a reference

    Hi,

    I need to align and call snps for a 14mb region of resequenced gDNA. I'm just thinking about the best way to construct my ref sequence. Exons, promoters,5' and 3' ends, conserved non-coding seqs and predicted alternative splicing sites have been selectively sequenced. Would the best approach be to just align against this whole section of hg18 using a gapped aligner as opposed to attempting to construct a ref sequence from parts of this region?

    thanks in advance
  • dnusol
    Senior Member
    • Jul 2009
    • 136

    #2
    I´d suggest you align against the whole genome and then just focus on your region of interest. This way you probaly avoid genomic duplications.

    HTH

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