General Discussion

About the General Discussion category (1)
Gneiss Differential Abundance Test Questions (2)
Dada2 chimera filtering and beyond (9)
Solving An Issue in Molecular Level (3)
Method comparison - differences in observed richness (2)
Filter by group or entire dataset? (7)
QIIME compatible taxonomic databases help (5)
Do the EMP 18S rRNA primers amplify bacteria as well? (4)
SILVA: why is chloroplast defined as bacteria? (7)
Using trimmomatic before qiime2 (2)
QIIME 1 and 2 returning completely different outputs (5)
Parameters Description (2)
Parameters are done In Order? (4)
DADA2 parameters, Data Quality is so poor (2)
Merging paired-end reads (2)
After using DADA2, needs to take OTUs? (6)
QIIME2 resource for developer (2)
Low quality forward reads (8)
What you Trimmomatic or quality control methods of qiime2? (3)
Number of samples and Frequency per samples Vs. Number of Features and Frequencies per Features (8)
Handling ambiguous nucleotides in database construction (7)
No understand the these parameters' concept (8)
Taxonomy assignment and rarefying (3)
How can i pull individual bacterial sequences from 16s processed data (9)
Filtering samples from sequencing run before running DADA2 (5)
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)