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Suppose that I have N long genomes (e.g. primates) and want to compute mappings between all pairs of the genomes. What is the best way to do so using mashmap? For example, is it a good idea to cat everything into a single FASTA file and then align it against itself, or it is the best to run the comparisons separately? And how would one adjust the parameters in such a case?
The text was updated successfully, but these errors were encountered:
You could go with either way... With the first approach, you may need additional post-processing of discarding mappings that span two genomes (in case they occur), so may be second is more convenient. Just pick the filtering criteria based on your application needs.
Hi,
Suppose that I have N long genomes (e.g. primates) and want to compute mappings between all pairs of the genomes. What is the best way to do so using mashmap? For example, is it a good idea to cat everything into a single FASTA file and then align it against itself, or it is the best to run the comparisons separately? And how would one adjust the parameters in such a case?
The text was updated successfully, but these errors were encountered: