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Reading in the silva.v123.align template sequences... DONE.
It took 22 to read 14914 sequences.
Aligning sequences from e.coli.16s.pcr.fasta ...
Reading in the silva.v123.align template sequences... Error in reading your fastafile, at position -1. Blank name.
DONE.
It took 0 to read 0 sequences.
The text was updated successfully, but these errors were encountered:
If number of processors was greater than number of sequences than we meant to adjust processors to number of sequences, but instead were adjusting to the number of file positions. The number of file positions is the number of sequences + 1. Rare bug caused empty file error.
#195
mothur > align.seqs(fasta=e.coli.16s.pcr.fasta, reference=silva.v123.align)
Using 4 processors.
Reading in the silva.v123.align template sequences... DONE.
It took 22 to read 14914 sequences.
Aligning sequences from e.coli.16s.pcr.fasta ...
Reading in the silva.v123.align template sequences... Error in reading your fastafile, at position -1. Blank name.
DONE.
It took 0 to read 0 sequences.
The text was updated successfully, but these errors were encountered: