Open fconstancias opened 1 year ago
Hello,
We recommend using QIIME 2's demux plugin's emp-paired or emp-single method, depending on whether your sequence data are paired or not.
https://docs.qiime2.org/2022.11/plugins/available/demux/
This approach will demultiplex your reads and trim primers and adapter sequences, but only works for data generated using the EMP protocol as you are. If other library construction methods are used we recommend using QIIME 2's cutadapt plugin for removing adapter and primer sequences.
Best wishes,
Justin
On Wed, Jan 18, 2023 at 12:48 AM Florentin Constancias < @.***> wrote:
Dear EMP protocol users,
We are using the EMP protocol (515F - 806R, forward-barcoded) to generate 16S libraries.
I am not sure which sequence/tool should I use for adaptor trimming when using the protocol. Do you have any recommendation?
Thanks
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-- Justin Shaffer, PhD Postdoctoral Researcher Rob Knight Group Department of Pediatrics, School of Medicine University of California, San Diego justinshafferbio.wordpress.com
Dear EMP protocol users,
We are using the EMP protocol (515F - 806R, forward-barcoded) to generate 16S libraries.
I am not sure which sequence/tool should I use for adaptor trimming when using the protocol. Do you have any recommendation?
Thanks