No sequences were mapped to samples. Check that your barcodes are in the correct orientation (see the rev_comp_barcodes and/or rev_comp_mapping_barcodes options). If barcodes are NOT Golay format set golay_error_correction to False.
Debug info has been saved to /var/folders/h1/7zgcmgzn3r3g30pq3s0k5zzh0000gn/T/qiime2-q2cli-err-3e9p6165.log
Please let me know how can i fix the above error
Thank you
Have you tried using the rev_comp_barcodes or the rev_comp_mapping_barcodes? You might want to unzip your barcodes fastq file and look at a few of the barcodes to confirm their orientation/formatting are what you expect them to be.
It is also worth finding out if the barcodes are Golay. If they are not you will want to set --p-no-golay-error-correction when running your analysis. You may need to ask your sequencing center and/or look through any documentation they provided you with to know if this is the case.