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I am using the below command to simulate reads from 3 draft genomes in separate multi-FASTA files, where each FASTA file represents one genome. The contig ids in each file are different from the FASTA file name.
The error traceback (attached file) has been traced using '--debug' option along with the above code
I would like to know about pre-processing draft FASTA files and how to specify abundances for each sample (and not each contig in the draft genome). Also can we specify the draft genomes in a single text file along with absolute paths? iss_error.log
.
The text was updated successfully, but these errors were encountered:
Hi,
I am using the below command to simulate reads from 3 draft genomes in separate multi-FASTA files, where each FASTA file represents one genome. The contig ids in each file are different from the FASTA file name.
genome_abundance.txt:
VB103 0.4
VB3985 0.2
VB7185 0.4
The error traceback (attached file) has been traced using '--debug' option along with the above code
I would like to know about pre-processing draft FASTA files and how to specify abundances for each sample (and not each contig in the draft genome). Also can we specify the draft genomes in a single text file along with absolute paths?
iss_error.log
.
The text was updated successfully, but these errors were encountered: