Hello!
I'm trying to cleanup my data but there's not enough overlap between forward and reverse samples. I've already increased the retaining area but still not enough overlap in a few samples. What should I do? Is there any code to remove such samples?
This is the error message: /var/folders/sm/q87dz81s50l651tfwfcf2vsc0000gn/T/qiime2-q2cli-err-h38dwv8x.log
Thanks!
Giovana
Hey @GioFranco,
Can you send a screenshot of your interactive quality plot?
Dada2 filters out the sequences that don't join so if after dada2 you have no sequences that means that they were all filtered out (possibly because they didn't join possibly for other quality reasons).
If there is no way to make the sequences overlap then you could run dada2 denoise-single and stick to a single end read analysis although I understand that is not preferable
@GioFranco,
Truncating your reverse reads just before your quality drop off near bp 225 might do the trick, but I am afraid you may end up having to use @cherman2's suggestion of performing a single end analysis.
@GioFranco,
Also, when the error message has been written to a log file like that, you can actually view it by copying the path/name of the file and running cat on it, your case that would look like:
> cat /var/folders/sm/q87dz81s50l651tfwfcf2vsc0000gn/T/qiime2-q2cli-err-h38dwv8x.log
and then copying and pasting the output here.
You also might be able to perform quality based filtering before denoising as seen here.
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