Closed goshng closed 6 months ago
The fasta_file_list option is useful if you have each single sequence in a separate fasta file. But what you have here is separate alignments of genes in each fasta file. To handle this, ClonalFrameML needs you to first put all the genes in a XMFA file and then use the xmfa_file option:
cat l1.fa > l.xmfa;echo = >> l.xmfa;cat l2.fa>>l.xmfa;echo = >> l.xmfa;cat l3.fa>>l.xmfa;echo = >> l.xmfa
Then you should run
ClonalFrameML tree.nwk l.xmfa cf_l -xmfa_file true
Hi,
I want to use -fasta_file_list opton because I have three alignment files in FASTA format: l1.fa, l2.fa, and l3.fa, and want to use them as blocks in ClonalFrameML. File
l.txt
has a line: l1.fa l2.fa l3.fa.I've attached a compressed file with the files that I tested. I tried the source code version and conda package version, and either produced the same error.
Did I misunderstand the usage of the option -fasta_file_list?
Thank you, SangChul
t.tar.gz