Simulate an SV VCF file based on a reference genome
meta
Groovy Map containing fasta information e.g. [ id:'test', single_end:false ]
[ id:'test', single_end:false ]
fasta
The reference genome
*.{fasta,fna,fa}
meta2
Groovy Map containing fasta index information e.g. [ id:'test', single_end:false ]
fai
The index of the reference genome
*.fai
meta3
Groovy Map containing parameters information e.g. [ id:'test', single_end:false ]
parameters
A text file containing the parameters to be used for the simulation. Gets automatically generated using defaults when this is not supplied
*.txt
snp_mutation_frequency
The SNP mutation frequency in the output VCF (0-1)
sim_reads
Whether or not to simulate reads (1==yes, else no)
Groovy Map containing sample information e.g. [ id:'test', single_end:false ]
versions
File containing software versions
versions.yml
The created parameters file
vcf
A VCF containing the simulated variants
*.vcf
bed
A BED file of the simulated structural variants
*.bed
A Fasta file file containing the variants from the output VCF
*.fasta
insertions
A Fasta file file containing insertion sequences
*.insertions.fa
Toolset for SV simulation, comparison and filtering
