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Fixing installation instructions
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conf/lsh.config

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params {
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max_cpus = 40
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max_ram = 250
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reference_base = "/projects/references/gmo-check"
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}
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// Resource manager settings

conf/resources.config

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genomes {
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tomato {
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fasta = "${params.reference_base}/solanum_lycopersicum.fa"
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fai = "${params.reference_base}/solanum_lycopersicum.fa.fai"
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dict = "${params.reference_base}/solanum_lycopersicum.dict"
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fasta = "${params.reference_base}/tomato/solanum_lycopersicum.fa"
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fai = "${params.reference_base}/tomato/solanum_lycopersicum.fa.fai"
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dict = "${params.reference_base}/tomato/solanum_lycopersicum.dict"
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amplicon_txt = "${baseDir}/assets/genomes/tomato/amplicon.txt"
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bed = "${baseDir}/assets/genomes/tomato/primers.bed"
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target_bed = "${baseDir}/assets/genomes/tomato/targets.bed"

docs/installation.md

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This pipeline requires locally stored genomes in fasta format. To build these, do:
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```
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nextflow run marchoeppner/gmo-check -profile standard,singularity --run_name build_refs --outdir /path/to/references
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nextflow run marchoeppner/gmo-check -profile standard,singularity --build_references --run_name build_refs --outdir /path/to/references
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```
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If you do not have singularity on your system, you can also specify docker, podman or conda for software provisioning - see the [usage information](usage.md).

docs/usage.md

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## `--outdir results` [default = results]
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The location where the results are stored. Usually this will be `results`in the location from where you run the nextflow process. However, this option also accepts any other path in your file system(s).
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The location where the results are stored. Usually this will be `results`in the location from where you run the nextflow process. However, this option also accepts any other path in your file system(s).
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## `--freebayes_min_alternate_count 50` [ default = 50]
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The minimum number of reads to support a given SNP. Since we are working with amplicon data, this value can be fairly high.
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## `--freebayes_min_alternate_frac 0.01` [ default = 0.01]
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The minimum percentage of reads supporting a SNP at a given site for the SNP to be considered. The default of 1% is chosen to be able to detect low levels of contribution but may need some tweaking depending on your exact sequencing setup and coverage.

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