Basic:
-r, --reference <FASTA>
Path to the FASTA file containing the reference genome. The same reference genome as was used for read alignment.-b, --bed <BED>
Path to the BED file with reference coordinates of tandem repeats-m, --mother <PREFIX>
Common (path) prefix of spanning reads BAM file and variant call VCF file of mother-f, --father <PREFIX>
Common (path) prefix of spanning reads BAM file and variant call VCF file of father-c, --child <PREFIX>
Common (path) prefix of spanning reads BAM file and variant call VCF file of child-o, --out <CSV>
Output csv path--trid <TRID>
Optionally a tandem repeat ID may be supplied, if so, only this site will be tested, default = None-@ <THREADS>
Number of threads, the number of sites that are processed in parallel, default = 1-h, --help
Print help-V, --version
Print version
Advanced:
--flank-len <FLANK_LEN>
Number of flanking nucleotides added to a target region during realignment, default = 50--no-clip-aln
Score alignments without stripping the flanks--parental-quantile <QUANTILE>
Quantile of alignment scores to determine the parental threshold, default is strict and takes only the top scoring alignment, default = 1.0--aln-scoring
Scoring function for 2-piece gap affine alignment (non-negative values): mismatch,gap_opening1,gap_extension1,gap_opening2,gap_extension2, default = "8,4,2,24,1", see here for more details on parametrization