I am pretty new to using qiime2 and I am trying to cut some sequences from my reads. For some reason qiime2 pops up with saying that my .fastq.gz file is not a QIIME archive. This is what I entered on the command line:
That warning is actually for a really good reason - QIIME archives and Artifacts are a core concept in QIIME 2. If you haven't had a chance to at least peek at the docs, now would be the time - you will save yourself a lot of heartache . I would suggest starting here: Overview of QIIME 2 Plugin Workflows — QIIME 2 2018.6.0 documentation
After you get up to speed there, check out this community tutorial:
I am trying to import my data and running qiime 2 on a VM. My code is on juypter notebook and having some syntax errors that I am not able to find. It looks like everything is spelled correctly tho.
Hey there @MAX_MIAO - can you please copy and paste the entire error message you received? You can re-run with the --verbose flag for that info. As well, sharing your manifest file would be helpful. Thanks!
I was able to figure out my error. I was just having some naming issues on my manifest file, there was a extra intended spacing. Just on another note tho, has this bug been solved yet? Cutadapt thinks my fastq.gz files aren't fastq.gz
because I am also facing the similar issue and now I am resorting to the plan cutadapt tool as you mentioned. My samples have been already demultiplexed for me and each sample has a R1 and R2 read for the forward and reverse reads respectively. And so, this is what I wrote for cutadapt:
cutadapt -a TCCTCCGCTTATTGATATGC --match-read-wildcards /home/qiime2/Greenhouse_experiment_2017/180612_BVDJ2/Gh_expt2017_A10{1,5}_S10{1,5}_L001_R1_001.fastq.gz > /home/qiime2/Greenhouse_experiment_2017/180612_BVDJ2/trimmed_16S/output.fastq
Does this look right? I want the standard output to go into a folder that I already made called “trimmed_16S”.