I've just started playing with the long read algorithm for bwa (dbwtsw), and I was wondering if it would be useful for aligning 454 or Sanger length cDNA reads back to a genomic assembly.
Back in the old days, I'd use wu-blast for this kind of thing, its ability to sort HSPs into alignment groups, and report only the most likely grouping of HSPs using topcomboN was tremendously helpful to me. I could layer my cDNAs onto genomic sequence, and in most cases blast could piece together alignments broken even by large introns.
I was wondering how bwa behaved in cases where a long (454-length) cDNA read spanned an intron in a genomic reference. Will this just drop the score so much that bwa won't even realize its an alignment? Or will it show the partial alignments of each end of the cDNA read to the seperated positions on the genomic reference in true 'local' fashion?
If bwa is not able to do this, can anyone suggest a modern aligner that can? Or should I just stick with blast and/or blat?
Back in the old days, I'd use wu-blast for this kind of thing, its ability to sort HSPs into alignment groups, and report only the most likely grouping of HSPs using topcomboN was tremendously helpful to me. I could layer my cDNAs onto genomic sequence, and in most cases blast could piece together alignments broken even by large introns.
I was wondering how bwa behaved in cases where a long (454-length) cDNA read spanned an intron in a genomic reference. Will this just drop the score so much that bwa won't even realize its an alignment? Or will it show the partial alignments of each end of the cDNA read to the seperated positions on the genomic reference in true 'local' fashion?
If bwa is not able to do this, can anyone suggest a modern aligner that can? Or should I just stick with blast and/or blat?
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