Hi There,
I am trying to look at the relative taxonomic abundance of bacteria in a given illumina sample so I want to load the data in then create a dada2 output and then follow this post. I am using the following code and running into an error "Importing 'SingleLanePerSamplePairedEndFastqDirFmt' requires a directory, not /home/boom/Desktop/qiime/manifest.csv"
Command:
qiime tools import \
--type 'SampleData[PairedEndSequencesWithQuality]'\
--input-path /home/boom/Desktop/qiime/manifest.csv \
--output-path /home/boom/Desktop/qiime/demux.qza
manifest.csv:
Sample-id,absolute-filepath,direction
#HB35,,
Sample-1,/home/boom/Desktop/qiime/HB35_R1.trimmed.fastq,forward
Sample-1,/home/boom/Desktop/qiime/HB35_R2.trimmed.fastq,reverse
I tried this with and without the # line. Do you have any suggestions?
Best,
Barry G.