Program versions and specific command line options. $1 = prefix for isolate $2 = path to reference genome in .fasta format ConDeTri perl condetri_v2.2.pl -fastq1= -fastq2= -prefix=$1 -hq=25 -lq=10 -frac=0.8 -minlen=50 -mh=5 -ml=1 -sc=33 perl filterPCRdupl_v1.01.pl -fastq1=$1_trim1.fastq -fastq2=$1_trim2.fastq -prefix=$1 -cmp=50 BWA-MEM v0.7.4 # before running, need to index reference genome: bwa index $2 bwa mem $2 $1_uniq1.fastq $1_uniq2.fastq >$1.sam Qualimap v2.0.2 qualimap bamqc -bam $1.bam -outdir SAMtools v0.1.19 # before running, need to index reference genome: samtools faidx $2 samtools view -uS -o $1.bam $1.sam samtools sort $1.bam $1 samtools index $1.bam samtools mpileup -P ILLUMINA -C50 -q20 -Q20 -uf $2 $1.bam | bcftools view -cg - > $1.vcf wgsim (simulating reads from sequences available on GenBank) wgsim -N 400000 -1 250 -2 250 MUMmer v3.23 repeat-match $2 > seq.repeats SPAdes v3.5.0 spades.py -k 55 --careful -1 $1_uniq1.fastq -2 $1_uniq2.fastq -o QUAST v2.3 python quast.py -R $2 -o PAGIT v1.64 (virtual machine downloaded March 3, 2015; iCORN2 downloaded separately) ABACAS v1.3.1 perl abacas.pl -r $2 -q <$1.fasta> -p nucmer -b -c -t -g $1_gaps -o $1 Image cat $1.fasta $1.contigsInbin.fas > $1_mappedAndUnmapped.fasta perl image.pl -scaffolds $1_mappedAndUnmapped.fasta -prefix $1 -iteration 1 -all_iteration 5 -dir_prefix ite -kmer 55 perl contigs2scaffolds.pl new.fa new.read.placed 300 500 $1_scaffolds iCORN2 v0.95 perl icorn2.sh $1 180 $1_scaffolds.fa 1 5 LS-BSR v3 Dependencies: Usearch v6.0.307, BLAST v2.2.25, prodigal v2.6.2 python ls_bsr.py -d -u python pan_genome_stats.py –b bsr_matrix_values.txt python BSR_to_PANGP.py –b bsr_matrix_values.txt python compare_BSR.py -1 -2 –f consensus.fasta –b bsr_matrix_values.txt PanGP-ubuntu-64bit-1.0.1 algorithm: Distance Guide sample size: 500 sample repeat: 10 amplification coefficient: 10 Gview BLAST parameters: filter low complexity sequences; value cut-off 1e-10; alignment length cutoff =100; percent identity cutoff = 80 Parsnp (Harvest v1.0.1) parsnp -r $2 -d -o -c BEDTools bedtools maskfasta -fi -bed -fo where bedfile is tab-delimited textfile: name of chromosome/node startpos endpos BratNextGen- bratPackage downloaded May, 2015 fixed hyperparameter α = 4 recombination estimation algorithm = 20 iterations estimate significance = 100 permutations significance α = 0.05 Gubbins v1.1.1 virtual machine run_gubbins.py gubbins_drawer.py -o -t PhyloPhlAn Dependencies: Usearch v5.2.32, FastTree, Muscle v3.8.31 python phylophlan.py -u fineSTRUCTURE v2.0.4 perl ./makeuniformrecfile.pl ChromoPainter-EM fs cp -in -i 10 -a 0 0 -j -g -r -o perl ./neaverage.pl -o ChromoPainter fs cp -a 0 0 -n -M -g -r -j -b -o chromoRun ChromoCombine fs combine -o -d perl ./chromopainterindivrename.pl fineSTRUCTURE fs fs -x 500000 -y 500000 -z 250 fs fs -x 50000 -m T SplitsTree v4.13.1 PhyML- run using Geneious plugin GTR model, gamma distribution, 1000 bootstrap replicates Path-O-Gen v1.4 MrBayes v3.2.5 lset nst=6 rates=Invgamma Ploidy =Haploid mcmc ngen=10000000 samplefreq =1000 printfreq =1000 BaTS v0.9 beta java -jar BaTS_beta_build2.jar single 100