| Miscellaneous |
| Version lineage of this tool (guids ordered most recent to oldest) |
| toolshed.g2.bx.psu.edu/repos/crs4/kggseq_variant_selection/kggseq_variant_selection/1.5 (this tool) |
| toolshed.g2.bx.psu.edu/repos/crs4/kggseq_variant_selection/kggseq_variant_selection/1.4 |
| toolshed.g2.bx.psu.edu/repos/crs4/kggseq_variant_selection/kggseq_variant_selection/1.3 |
| toolshed.g2.bx.psu.edu/repos/crs4/kggseq_variant_selection/kggseq_variant_selection/1.2 |
| toolshed.g2.bx.psu.edu/repos/crs4/kggseq_variant_selection/kggseq_variant_selection/1.1 |
| kggseq_variant_selection |
| Requirements (dependencies defined in the <requirements> tag set) |
| name | version | type |
| kggseq | 1.0_20180410 | package |
| Additional information about this tool |
java -jar \$KGGSEQ_JAR_PATH/kggseq.jar
## Environmental settings
--buildver hg19
--resource \$KGGSEQ_JAR_PATH/resources
--no-lib-check
--no-resource-check
--no-progress-check
--out results
--o-vcf
--no-gz
--vcf-file $inputFile
--ped-file $pedFile
--db-gene $db_gene
$composite_subject_id
## Variant and genotype filters
#if str($variant_genotype_filters.variant_genotype_filters_select) == "yes"
$variant_genotype_filters.pass_variant_only
--seq-qual $variant_genotype_filters.seq_qual
--seq-mq $variant_genotype_filters.seq_mq
--seq-sb $variant_genotype_filters.seq_sb
--seq-fs $variant_genotype_filters.seq_fs
--min-heta $variant_genotype_filters.min_heta
--min-homa $variant_genotype_filters.min_homa
--min-hetu $variant_genotype_filters.min_hetu
--min-homu $variant_genotype_filters.min_homu
--min-obsa $variant_genotype_filters.min_obsa
--min-obsu $variant_genotype_filters.min_obsu
--min-obs $variant_genotype_filters.min_obs
#if str($variant_genotype_filters.hwe_control)
--hwe-control $variant_genotype_filters.hwe_control
#end if
#if str($variant_genotype_filters.hwe_case)
--hwe-case $variant_genotype_filters.hwe_case
#end if
#if str($variant_genotype_filters.hwe_all)
--hwe-all $variant_genotype_filters.hwe_all
#end if
--gty-qual $variant_genotype_filters.gty_qual
--gty-dp $variant_genotype_filters.gty_dp
--gty-sec-pl $variant_genotype_filters.gty_sec_pl
--gty-af-ref $variant_genotype_filters.gty_af_ref
--gty-af-het $variant_genotype_filters.gty_af_het
--gty-af-alt $variant_genotype_filters.gty_af_alt
#else
--no-qc
#end if
## Genetic inheritance
#if str($genetic_filters.genetic_filters_select) == "yes"
#if str($genetic_filters.genetic_model.genetic_model_select) == "yes"
#if $genetic_filters.genetic_model.custom_genetic_params
--genotype-filter $genetic_filters.genetic_model.custom_genetic_params
#end if
#else
$genetic_filters.genetic_model.suggested_genetic_params
#end if
#end if
## Homozygosity - IBS - IBD filters
#if str($hom_ibs_ibd_filters.hom_ibs_ibd_filters_select) == "yes"
#if str($hom_ibs_ibd_filters.homozygosity_case_filter)
--homozygosity-case-filter $hom_ibs_ibd_filters.homozygosity_case_filter
#end if
#if str($hom_ibs_ibd_filters.ibs_case_filter)
--ibs-case-filter $hom_ibs_ibd_filters.ibs_case_filter
#end if
#if str($hom_ibs_ibd_filters.ibd_annot) != 'None'
--ibd-annot $hom_ibs_ibd_filters.ibd_annot
#end if
#end if
## Gene feature filters
#if str($gene_feature_filters.gene_feature_filters_select) == "yes" and $gene_feature_filters.gene_features
--gene-feature-in $gene_feature_filters.gene_features
--splicing $gene_feature_filters.splicing
--neargene $gene_feature_filters.neargene
#end if
## Common variants filters
#if str($allele_freq_filters.allele_freq_filters_select) == "yes"
#if $allele_freq_filters.allele_freq_db
--db-filter $allele_freq_filters.allele_freq_db
#end if
--rare-allele-freq $allele_freq_filters.rare_allele_freq
#end if
## Genomic regions filters
#if str($genomic_region_filters.genomic_region_filters_select) == "yes"
$genomic_region_filters.ignore_indel_or_snv
#if $genomic_region_filters.regions_in
--regions-in "$genomic_region_filters.regions_in"
#end if
#if $genomic_region_filters.regions_out
--regions-out "$genomic_region_filters.regions_out"
#end if
#if $genomic_region_filters.genes_in
--genes-in "$genomic_region_filters.genes_in"
#end if
#if $genomic_region_filters.genes_out
--genes-out "$genomic_region_filters.genes_out"
#end if
$genomic_region_filters.superdup
#if str($genomic_region_filters.gene_var_filter)
--gene-var-filter $genomic_region_filters.gene_var_filter
#end if
#end if
## Predicted impact filters
#if str($impact_filters.impact_filters_select) == "yes"
--db-score dbnsfp
$impact_filters.filter_nondisease_variant
$impact_filters.mendel_causing
#end if
## Add annotations
#if str($add_annotations.add_annotations_select) == "yes"
#if str($add_annotations.o_flanking_seq)
--o-flanking-seq $add_annotations.o_flanking_seq
#end if
$add_annotations.genome_annotation
$add_annotations.omim_annotation
$add_annotations.cosmic_annotation
$add_annotations.scsnv_annotation
$add_annotations.dgv_cnv_annotation
$add_annotations.superdup_annotation
$add_annotations.mouse_pheno_annotation
$add_annotations.zebrafish_pheno_annotation
$add_annotations.ddd_annotation
$add_annotations.patho_gene_predict_annotation
#if $add_annotations.pubmed_mining_gene
--phenotype-term "$add_annotations.pubmed_mining_gene" --pubmed-mining
#end if
#if str($add_annotations.shared_genes.shared_genes_select) == "yes"
--ppi-annot string
--candi-file $add_annotations.shared_genes.candi_file
--ppi-depth $add_annotations.shared_genes.ppi_depth
--pathway-annot $add_annotations.shared_genes.pathway_annot
#end if
#end if
> $logFile
| Functional tests |