Hey everyone! Hope you're well!
Very new to this wonderful world of sequencing analysis!
Basically, as a result of Ion Torrent sequencing of 24 samples of 16S V6 rRNA I have fastq files (barcodes and primers have already been removed).
I carried out basic quality end trimming and passed them through a quality filter using the fastx_toolkit.
Now I want to map these 'cleaned' reads using mothur but I have NO idea where to start!
Help!!!!!
Very new to this wonderful world of sequencing analysis!
Basically, as a result of Ion Torrent sequencing of 24 samples of 16S V6 rRNA I have fastq files (barcodes and primers have already been removed).
I carried out basic quality end trimming and passed them through a quality filter using the fastx_toolkit.
Now I want to map these 'cleaned' reads using mothur but I have NO idea where to start!
Help!!!!!
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