I need help with a import command for merged_reads.fq
The sequencing center has not provided individual fastq files for analysis. They sent data as merged_reads.fq format. How do I import this into qiime?
Usually I create raw reads folder that contains FASTQ files for each sample and then use this command:
qiime tools import
--type 'SampleData[PairedEndSequencesWithQuality]'
--input-path
--input-format CasavaOneEightSingleLanePerSampleDirFmt
--output-path demux-paired-end.qza
How should I edit the above command for merged_reads.fq?
Good question! Here's a really helpful answer from @cherman2 regarding importing pre-merged sequences, along with some resources for performing quality control on your data: