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population-diversity:microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data

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population-diversity:microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data [2020/04/29 10:14] – [Qiime2 data filtering and feature (OTU) table construction] bnginapopulation-diversity:microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data [2020/04/29 13:35] bngina
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 To see usage and parameters that can be adjusted get the help for the pluggin i.e To see usage and parameters that can be adjusted get the help for the pluggin i.e
  
 +<code>
 +qiime dada2 --help
 +</code>
  
 +The data we are using is paired-end, hence we will use the [[https://docs.qiime2.org/2020.2/plugins/available/dada2/|qiime dada2 denoise-paired]] pluggin. 
 +
 +A key parameter to be careful is the //''--p-trunc-q''//
 +Key parameters in quality control of the sequences are those used to trim the forward, ''--p-trim-left-f''; ''--p-trunc-len-f'' and reverse '' --p-trim-left-r''; ''--p-trunc-len-r'' reads. The //--p-trim-left-[f/r] tell qiime how many bases to trim from the beginning of the sequence, while the //--p-trunc-len[f|r] tell qiime at what position the sequences should be truncated at the end. 
population-diversity/microbiome-analysis-with-qiime2-using-illumina-paired-end-sequence-data.txt · Last modified: 2020/04/29 15:09 by bngina