Muscle seqaln( ) in linux vs Windows?
Issue #552
resolved
I used seqaln() in Windows. I had no problem. But when I used it with the same proteins in linux, seqaln() returns different and wrong results. How is this possible?
I have a list of proteins. In a for loop i execute read.fasta() for each protein and seqaln() with a pdb fasta sequence corresponding to each protein. I had no issue in Windows. But, in linux seqaln() is done with the previous protein fasta not the current one.
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This should not happen but it is impossible for us to investigate and solve your issue as you don't provide enough information for us to reproduce.
Note in particular the last point from the posting guide displayed when you clicked on "create issue".
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