Showing the last 30 topics from:

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Why are my reads filtered out (98%) when quality seems okay?654Thu Aug 20 2026
Why truncate with dada2 when ITSxpress is an option?16240Mon Aug 17 2026
PacBio ITS workflow - some questions380Mon Aug 17 2026
Request: DADA2 denoise-ccs without --p-front parameter251Tue Aug 04 2026
Is my truncation parameter exploration sufficient, and is my interpretation correct?153Tue Jul 28 2026
Losing reads at DADA2 Merge step 30% of my samples lost over 50% - I have tried multiple steps to fix- please help139Tue Jul 21 2026
Can DADA2 be used with nearly uniform Q38 quality scores?255Tue Jul 21 2026
Sequencing platform fully confounded with study period: MiSeq vs NextSeq 2000 (16S rRNA V3-V4)381Tue Jul 07 2026
QIIME 2 processing of MiSeq i100 data with constant quality scores3133Mon Jun 08 2026
Running DADA2 on pre-processed data7131Wed Jun 03 2026
Query about false read merging or no read merging141Tue May 26 2026
Merging NGS with TGS?365Wed May 20 2026
Under the hood of the "Moving Pictures" tutorial0168Wed May 13 2026
sequence alignment576Mon May 11 2026
An error was encountered while running DADA2 in R (return code 1), inspect stdout and stderr to learn more10130Fri May 08 2026
Help - DADA2 microbiome analysis372Mon May 04 2026
Qiime version and singletons386Mon Apr 27 2026
High number of unique sequences in PacBio full-length 16S CCS data with DADA22127Fri Apr 24 2026
Low overlap due to poor reverse read quality in 2×300 bp V3–V4 amplicon sequencing (DADA2)176Mon Apr 13 2026
High but variable sequence loss (32-68%) during DADA2 filtering with V3-V4 amplicons (MiSeq 600 cycles)2112Thu Apr 09 2026
Inadequate overlap for V3-V4 (paired-end) due to quality drop5127Mon Mar 09 2026
Integrating V3-V4 and V4 16S datasets for large-scale meta-analysis: Is Greengenes2 the optimal choice for cross-region alignment?1159Fri Mar 06 2026
Too many elements for DADA2 - denoise in batches?6147Wed Mar 04 2026
Analysis with DADA2... Merge Read Length164Wed Mar 04 2026
denoise failure582Tue Feb 24 2026
Huge difference of DADA2 output with and without removing primers4121Tue Jan 27 2026
Advice in best practice for handling multiple sequencing runs and subset analyses in QIIME 2 (DADA2)2126Fri Jan 16 2026
pair ended demultiplexed qza file causing strange error.165Sun Dec 28 2025
High read loss due to artifacts and chimera after denoising 16S V3-V4 paired-end reads181Wed Dec 17 2025
Denoising low quality reverse reads in paired-end sequencing reads4109Wed Dec 03 2025