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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
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