Hi,
Actually I have two questions related to MaltExtract output:
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Once I’ve run MaltExtract to identify ancient reads, is there a way to output the reads that map to specific taxa in fasta format for further analysis? Alternatively, can you form a rma file with just ancient reads?
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When MaltExtract is asked to identify reads at a target genus, does it summarise the reads that map best to that taxon as well as all the sub-taxa below it, or does it only look at the reads that map best at that level and can’t be placed any lower?
Thanks,
Hannah