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Drag out certain reads based on SingleM classification? #189
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Hi, If you run pipe with --otu-table and --output-extras it gives you the reads contained within each OTU. Is that what you mean? |
Hi Ben,
Thanks for the quick response. In the OTU table that you mentioned only contains 60 bases since singlem classified taxonmy according to this right? I mean like if there is a way I can know the original reads (150 bp reads by Illumina sequencing)?
Thanks a lot!
Best,
Shiyi
… On Jul 9, 2024, at 19:44, Ben J Woodcroft ***@***.***> wrote:
Hi,
If you run pipe with --otu-table and --output-extras it gives you the reads contained within each OTU. Is that what you mean?
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With output extras there is another column with the full read. It is also in the archive otu table output if you prefer json. |
Thanks a lot! I will give it a try!
… On Jul 9, 2024, at 20:07, Ben J Woodcroft ***@***.***> wrote:
With output extras there is another column with the full read. It is also in the archive otu table output if you prefer json.
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Hi SingleM team! I was wondering is it possible to drag out certian reads or know which reads are based on the taxonomy classification of SingleM? I am current consider using a smaller group of reads for metagenomic assembly/binnning process and curious about whether it is possible to use singleM to perform the first step.
Thanks in advance!
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