yes try bowtie with -v 0 parameter to set the number of mismatches to 0
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Hi,
Can anyone suggest an aligner which can handle mapping very short reads (<20 bp) to a reference genome?
Thank you.
I think you can use any of the short reads aligners. Just be careful to set number of mismatches to 0 or 1 and maybe disable indels, as @ 20bp sequence length the probability of random match is quite high. That depends of course on the size of your genome.
What is your reference genome size?
yes try bowtie with -v 0 parameter to set the number of mismatches to 0
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What kind of experiment? RNA-seq? Genome ?
What kind of experiment? RNA-seq? What genome? bacteria ?
And how many reads?