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hi doctor, I would like to ask if there are any special processing steps required for analyzing amplicon data such as 16S V3-V4 using Kraken2, aside from the regular data quality control (e.g., removing low-quality bases and adapters), such as removing primer sequences from paired-end reads and merging the paired-end reads before inputting the results into Kraken2 for analysis?
Lu J, Salzberg S L. Ultrafast and accurate 16S rRNA microbial community analysis using Kraken 2[J]. Microbiome, 2020, 8(1): 124.
The text was updated successfully, but these errors were encountered:
hi doctor, I would like to ask if there are any special processing steps required for analyzing amplicon data such as 16S V3-V4 using Kraken2, aside from the regular data quality control (e.g., removing low-quality bases and adapters), such as removing primer sequences from paired-end reads and merging the paired-end reads before inputting the results into Kraken2 for analysis?
Lu J, Salzberg S L. Ultrafast and accurate 16S rRNA microbial community analysis using Kraken 2[J]. Microbiome, 2020, 8(1): 124.
The text was updated successfully, but these errors were encountered: