Hi,
I have from MiSeq FASTQ files, pair-end, of 16s bacterial amplicons. I want to start a metagenomics analysis and I have read that most of the time people use Mothur or Qiime.
But for example Qiime needs the FASTQ files and also mapping file. My case is that I have only the R1 and R2 pair-end files for each sample which are already demultiplexed (from MiSeq) with removed barcodes and primers.
So was wondering how can I proceed from what I have already?
Thanks
Thanks but in the case I do not know the primers and barcode (they are already removed from the company) how to do that?
Here is an example from qiime:
Mapping Files Without Barcodes and/or Primers
In some circumstances, users may need to generate a mapping file that does not contain barcodes and/or primers. To generate such a mapping file, fields for “BarcodeSequence” and “LinkerPrimerSequence” can be left empty. An example of such a file is below (note that the tabs are still present for the empty “BarcodeSequence” and “LinkerPrimerSequence” fields):
http://qiime.org/documentation/file_formats.html
Best, Agata