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controlsConfigTemplate.yaml
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###input files
bamList: BAMLIST ###path to file contining path to bams
regionsFile: BEDFILE ###path to bed file defining regions targeted in exome
refGenome: REFGENOME ###path to reference genome that was used to align bams
snpVCFpath: VCFPATH ###path to vcfs containg popuulation frequencies (one for each chromosome),
###including part of filename before chromosome number
snpVCFname: VCFNAME ###filename/extension of population vcf following chromosome number
###user inputs
sexList: SEXLIST ###comma deliminated list of sex for each bam in the bamlist in the same order
gvmPath: GVMPATH ###path to folder containing gvm executable
outfile: OUTFILE ###path and name of output
###organism specific parameters
###values below are set for human
autosomes: "1:22" ####range of numbers for autosomal chromosmes 1:maxAutosome
sexChr: X,Y #### comma separated list of sex chromosomes
F: 2,0 #### number of copies of sex chr for individuals of sex F
M: 1,1
###advanced parameters - most users should keep default belows below
mpileupC: 50 ####mpileupC parameter
pvFreq: 1E-5 ####expected frequency of private SNPs
pvFreqIndel: 1E-6 ####expected frequency of private indels
minMQ: 10 ####minimum mapping quality to count read
defaultBQ: 30 ####BQ used for indels
defaultMQ: 40
BQoffset: 33 ####used for translation ascii to scores
MQoffset: 33 ####used for translation ascii to score
priorMapError: 0.03 ####prior probability genotype cannot be determined at postion
#### number of copies of sex chr for individuals of sex M