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Thanks for developing this. I had a question about the output files and, after reading the README, I am still unsure on the expected output.
I am using PE150 MiSeq reads. Performed a SPAdes assembly (this output is *.scaffolds.fasta). These genomes are highly fragmented but >99% ANI to a reference genome that I have previously sequenced fully with PACBIO (complete genome; 3.77Mb). However, when I use AlignGraph, the output files confuse me.
This appears to me that I would need to concatenate the *extended.fasta with the *remaining.fasta file to get the desired genome? Any clarification would be great.
Sorry for reply late. Yes, the extended.fasta file contains extended contigs by AlignGraph, and the remaining.fasta file contains the not extended contigs.
Hi,
Thanks for developing this. I had a question about the output files and, after reading the README, I am still unsure on the expected output.
I am using PE150 MiSeq reads. Performed a SPAdes assembly (this output is *.scaffolds.fasta). These genomes are highly fragmented but >99% ANI to a reference genome that I have previously sequenced fully with PACBIO (complete genome; 3.77Mb). However, when I use AlignGraph, the output files confuse me.
One example:
This appears to me that I would need to concatenate the *extended.fasta with the *remaining.fasta file to get the desired genome? Any clarification would be great.
Here is the command I am using:
Thank you!
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