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Quick Start
hanfc edited this page Sep 8, 2026
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This guide describes standard assembly workflows for organellar genomes using PMAT2.
HiFi reads offer high single-molecule accuracy. Assembly can be performed directly without pre-correction:
PMAT autoMito -i hifi.fastq.gz -o hifi_assembly -t hifi -m -T 8Key options:
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-t hifi: Specifies PacBio HiFi sequencing mode. -
-m: Keeps sequence data in memory to reduce disk I/O and speed up computation. -
-T 8: Allocates 8 CPU threads.
ONT reads require error correction before assembly. You can specify NextDenovo or Canu:
# Using NextDenovo for error correction
PMAT autoMito -i ont.fastq.gz -o ont_assembly -t ont -S nextdenovo -N /path/to/nextDenovo -m -T 8
# Using Canu for error correction
PMAT autoMito -i ont.fastq.gz -o ont_assembly -t ont -S canu -C /path/to/canu -m -T 8Continuous Long Reads (CLR) also require error correction:
PMAT autoMito -i clr.fastq.gz -o clr_assembly -t clr -S canu -C /path/to/canu -m -T 8By default, PMAT2 targets plant mitochondrial genomes (-G mt -x 0). You can adjust target organelles and taxonomy:
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-G mt: Assemble mitochondrial genome (default). -
-G pt: Assemble chloroplast (plastid) genome. -
-G all: Assemble both mitochondrial and chloroplast genomes. -
-x 0: Plants (default). -
-x 1: Animals. -
-x 2: Fungi.
Example (Animal Mitochondria):
PMAT autoMito -i animal_hifi.fq.gz -o animal_mt -t hifi -G mt -x 1 -m -T 8