MicroSeq is a microbiology-focused Sanger workflow for turning raw AB1 or FASTQ reads into QC-passed sequences, paired assemblies when appropriate, BLAST results, taxonomy-aware tables, and optional downstream BIOM outputs.

If you are using MicroSeq for 16S isolate identification or related microbiology workflows, this page is the best place to start.

Where should I start?

Most microbiology users

If you are working with paired forward/reverse Sanger reads

If you are running from a terminal, remote server, or HPC

Advanced and reference pages

Tiny glossary

Term Meaning
Q-cov Query coverage. This is the percentage of your query sequence covered by the alignment to a database hit.
contig A merged consensus sequence built from overlapping read evidence, such as forward and reverse reads from the same sample.
singlet A standalone sequence record that remains usable when a defended merged contig was not produced.
pair_missing A paired-mode outcome where only one direction survived pairing, so the sample never had a valid forward/reverse assembly opportunity.
filename primer labels The labels in the filename, such as 27F or 1492R, that MicroSeq uses to recognize forward and reverse files during pairing.

Quick launch

For most local microbiology users, the GUI is the easiest starting point:

```bash conda activate MicroSeq microseq-gui