Hi everyone,
I am working with a new sequencing center and I run into the problem that I never worked on a manifest document. I review the documents available on qiime and validate my manifest at keeime.
Carmen:FASTQ CarmenP$ qiime tools import --type 'SampleData[SequencesWithQuality]' --input-path manifest.txt --output-path single-end-demux.qza --input-format PairedEndFastqManifestPhred33
I get the following output
An unexpected error has occurred:
No transformation from <class 'q2_types.per_sample_sequences._format.PairedEndFastqManifestPhred33'> to <class 'q2_types.per_sample_sequences._format.SingleLanePerSampleSingleEndFastqDirFmt'>
See above for debug info.
I have three columns for my manifest: sample-id, fastq.path, and forward/reverse
The company told me that the FASTQ variant format is the default Illumina output: Phred33.
Anyone who has been running into the same problem? Any tips.
I am working from a mac using the terminal qiime2-2022.8 version
Thank you!