General Discussion


About the General Discussion category (1)
Filtering samples from sequencing run before running DADA2 (5)
How can i pull individual bacterial sequences from 16s processed data (3)
Distance Matrix and features (2)
Identifying bacterial taxa (16S) that correlate with eukaryotic taxa (18S) (8)
Taxonomic drivers (5)
Filter representative FASTA sequences (4)
Using read counts for abundance analysis (8)
Why does Greengenes assign more features at the class and order ranks than Silva? (1)
Minimum read for denoising process (5)
Working on functional gene- providing a database (2)
I'm loosing too many OTUs with taxa filter-table (~80%)--is this a normal/common phenomenon? (9)
Viewing reads before denoising (2)
Question about analyzing many samples (3)
Interpreting PC in beta-diversity (3)
Best approach for analyzing Sanger sequences from ITS2 region (11)
Comparing beta diversity between samples (not groups) (6)
Approaches to functional profile assessment (3)
Discussion: methods for removing contaminants and cross-talk (20)
16s circular phylogenetic tree (2)
Effect of not preparing data before DADA2 (9)
Any upcoming workshops? (3)
Taxonomy Analysis questions (9)
Potential artifacts produced with DADA2 wrapped in qiime2-2018.8 - need advice (7)
Taxonomic completenes, missingness in BOLD COI database (2)
What is the definition of sequence variants? (1)
Qiime moving picture data (2)
Mycobiome_ITS_Remove primers & barcode sequence (2)
Split_otu_table_by_taxonomy.py equivalent in Qiime 2 (2)
Number of basepair to trim in DADA2? (3)