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@@ -38,37 +38,40 @@ if [[ -z "$2" ]]; then
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# most of this file is comments, which you can delete #
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#=======================================================#
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fragment_size: 50
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fragment_size: 150
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# size of the sliding window genome fragments
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# values of 50-300+ should be ok (use your judgement)
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# note: bwa isn't good at mapping really long sequences
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reference_genome: ""
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reference_genome: "genome.fasta"
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# name of reference genome in the genomes/ dir
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outgroup: ""
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outgroup: "outgroupgenome.fasta"
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# name of the outgroup genome in the genomes/ dir
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bwa_parameters: "-a -k 19"
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# -a outputs all alignments
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# -k 19 is a kmer size of 19
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freebayes_parameters: "-C 1 --min-coverage 5 --standard-filter --ploidy 1"
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# -C 1 means at least 1 sample needs to have alt allele for a site to be kept
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# -C 2 means at least 2 samples need to have alt alleles for a site to be kept
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# --min-coverage 5 means at least 5 aligments to score a site
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# --standard-filter is equivalent to -m 30 -q 20 -R 0 -S 0
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# --standard-filter is to add more stringency
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# --ploidy 1 because these are typically haploid assemblies
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window_size: 50000
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sites_per_window: 10
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window_size: 20000
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# window size in base pairs for LD pruning snp data
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# bigger window = fewer snps
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sites_per_window: 10
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# number of sites to keep per window
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musclev5_parameters: "-replicates 100"
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# if runtime is important, you may want to reduce replicates
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mafft_parameters: "--auto --maxiterate 1000 --nuc"
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# --auto chooses the appropriate model for the data size
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# --maxiterate is the max number of iterations for tree building
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# --nuc is to specify the input is nucleotides
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raxml_model: "GTR+G"
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# the phylogenetic model you would like to use see for options:
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# the phylogenetic model you would like to use, see for options:
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# https://isu-molphyl.github.io/EEOB563/computer_labs/lab4/models.html
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raxml_parameters: '--bs-trees 100 --tree pars\{25\},rand\{25\} -brlen scaled'

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