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https://github.com/linsalrob/atavide_lite

A simpler version of atavide that relies only on slurm or PBS scripts. Some of the settings maybe specific for our compute resources
https://github.com/linsalrob/atavide_lite

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A simpler version of atavide that relies only on slurm or PBS scripts. Some of the settings maybe specific for our compute resources

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README

          

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# atavide lite

A simpler version of atavide that relies only on slurm or PBS scripts. Some of the settings maybe specific for our compute resources

[atavide](https://github.com/linsalrob/atavide) is a full-fledged metagenome processing pipeline. This is a simpler version that uses either slurm scripts or PBS scripts to accomplish the same things. In this initial release, we avoided snakemake to work through the steps one at a time, although that will likely come soon.

# Pipeline steps

1. Run fastp to trim Illumina adapters
2. Use `minimap2` and `samtools` to filter out host and not host reads. Currently host reads are ignored. Host can be human or anything else.
3. Use `mmseqs easy-taxonomy` to compare not host reads to UniRef. By default we use UniRef50 but you could use any version.
4. Create a taxonomic summary for each sample and make a single `.tsv` file.
5. Connect in the subsystems from BV-BRC, and make a table that includes subsystems and taxonomic information
6. Create a subsystems taxonomy for the data

# different versions

See the verions:
- [slurm](slurm/README.md) - designed to work on Flinders deepthought infrastructure
- [pbs](pbs/README.md) - designed to work on the NCI infrastructrue for now
- [minion pawsey](minion_pawsey)

Currently the pipeline depends on these software

- fastp
- samtools
- minimap2
- megahit
- mmseqs
- vamb

You can install all of these with:

```
mamba env create -f ~/atavide_lite/atavide_lite.yaml
```

If you use atavide light, please [cite it](citation.cff) and then please also [cite the other papers](references.bib) that describe these great tools.