Entering edit mode
22 months ago
Hello! My name is Andrea and currently I am working with SARS-CoV-2 sequences, in order to identify different quasispecies within given samples. Thereby, I would like to know if I could map the fasta files that I obtain as ouput of my process (corresponding every fasta to a different low-frequency variant identified in the same sample) to the SARS-CoV-2 canonical reference genome.
Thanks in advance!
If your fasta sequences are long then consider using a different aligner that can look for local alignments or be sure to add
--local
flag tobowtie2
.