You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
There is a small R script in the current NGS16S pipeline which extracts from the dada2.rda file the sequences which were dropped as chimeras and outputs a csv with columns weight and sequence. This file is not used for any downstream classification pipeline dependencies, however is useful to have for troubleshooting when a larger fraction of reads is lost during the chimera removal phase. The script currently outputs a file for each sample in the run, but it is not necessary to separate per sample if that is less convenient for the nextflow pipeline
I've got changes in #49 to complete this issue. Need to find a sample which demonstrates significant abundance of chimera and add that to the ngs16s test data set. /cc @nhoffman
There is a small R script in the current NGS16S pipeline which extracts from the
dada2.rda
file the sequences which were dropped as chimeras and outputs a csv with columnsweight
andsequence
. This file is not used for any downstream classification pipeline dependencies, however is useful to have for troubleshooting when a larger fraction of reads is lost during the chimera removal phase. The script currently outputs a file for each sample in the run, but it is not necessary to separate per sample if that is less convenient for the nextflow pipelineThe text was updated successfully, but these errors were encountered: