Previously, when users concatenated allele sequences, they were sorted alphabetically by genomic sequence. In a small number of cases, these meant that the genes came out in a different order which made comparing the output from different samples annoying. Following this change, the sequences are sorted by the name of their allele.
I had a quick look for something to turn a fasta into a phylip and hacked a one off python script. Any suggestions of a good tool for next time would be great.
Previously, when users concatenated allele sequences, they were sorted alphabetically by genomic sequence. In a small number of cases, these meant that the genes came out in a different order which made comparing the output from different samples annoying. Following this change, the sequences are sorted by the name of their allele.
I had a quick look for something to turn a fasta into a phylip and hacked a one off python script. Any suggestions of a good tool for next time would be great.