WISARD[wɪzərd] Workbench for Integrated Superfast Association study with Related Data |
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Column | Format | Modifier | Description | CHR | Positive integer | NONE | The rank of least conditional variance | VARIANT | Positive integer | NONE | The rank of least conditional variance | POS | Positive integer | NONE | The rank of least conditional variance | ALT | Positive integer | NONE | The rank of least conditional variance | ANNOT | Positive integer | NONE | The rank of least conditional variance | GENO | integer/integer/integer | NONE | Number of alleles for each of aa/Aa/AA, respectively | O(HET) | integer | NONE | Observed number of heterozygotes | E(HET) | real | NONE | Expected number of heterozygotes | STAT_HWE | real | NONE | Statistic of Hardy-Weinberg Equilibrium test | P_HWE | real | NONE | Exact p-value of HWE test | NIND | integer | NONE | Incorporated number of individuals for the test |
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Suffix | Format | Produced by | Affected by | Description | log | arbitrary | NONE | --verbose | A complete log file produced from an execution of WISARD | gene.res | TSV | --genetest | --skat --skato --pedcmc |
A result of gene-level test (Burden, SKAT, SKAT-o, PEDCMC) | simple.qls.res | TSV | --qls | NONE | A result of QLS analysis | extended.qls.res | TSV | --mfqls | --mqlsconsec | A result of Extended QLS analysis | all.hwe | TSV | --hwe all | NONE | A computed HWE using all samples | founders.hwe | TSV | --hwe founder | NONE | A computed HWE using only founder samples | sampvar.res | TSV | --sxa | NONE | A result of computation of conditional variance for each sample | top.sampvar.res | TSV | --sxa | --nsamp An ascending-sorted result of conditional variances | AI.blup | TSV | --makeblup | --nostop --emcount --aithr |
An estimation of BLUP using EM-AI algorithm for REML model | NR.blup | TSV | --makeblup --ml |
--nostop --emcount |
An estimation of BLUP using Newton-Raphson algorithm for ML model | SD.blup | TSV | --makeblup --specdcmp |
NONE | An estimation of BLUP using spectral decomposition | trend.res | TSV | --trend | NONE | A result of Cochran-Armitage trend test and allelic based test for the testing of association in case/control dataset | fisher.res | TSV | --fisher | NONE | A result of Fisher's exact test for the testing of association in case/control dataset | summary.variant.res | TSV | --variantsummary | NONE | A chromosome-wise summary for the various information from variants | tstv.variant.lst | TSV | --tstv | NONE | A result of Ts/Tv ratio by window | tstv.chr.lst | TSV | --tstv | NONE | A result of Ts/Tv ratio by chromosome | mistest.res | TSV | --mistest binary phenotype |
NONE | A result of test of random missingness between case/control | inbreed.coef.res | TSV | --inbreed | NONE | A result of computation of inbreeding coefficient F | lod.res | TSV | --lod | NONE | A result of Log of Odds analysis | mendel.sample.res | TSV | --mendel | NONE | A result of analysis of sample-wise Mendelian transmission error | mendel.variant.res | TSV | --mendel | NONE | A result of analysis of variant-wise Mendelian transmission error | mendel.family.res | TSV | --mendel | NONE | A result of analysis of family-wise Mendelian transmission error | sample.miss.lst | TSV | --miss | NONE | A report of genotype missingness per sample | variant.miss.lst | TSV | --miss | NONE | A report of genotype missingness per variant | family.miss.lst | TSV | --miss | NONE | A report of genotype missingness per family | tdt.res | TSV | --tdt | NONE | A result of Transmission Disequilibrium Test | sdt.res | TSV | --sdt | NONE | A result of Sibship Disequilibrium Test | fst.res | TSV | --fst | --set | A result of FST estimation | variant.popuniq.res | TSV | --popuniq | NONE | A list of population-specific variants | variant.famuniq.res | TSV | --famuniq | NONE | A list of family-specific variants | variant.singleton.res | TSV | --singleton | NONE | A list of singleton variants (it means, there is only 'one' sample who having variant allele in a variant across final dataset) | variant.monotone.res | TSV | --monotone | NONE | A list of monotone variants (it means, there is no sample who having variant allele in a variant across final dataset) | variant.doubleton.res | TSV | --doubleton | NONE | A list of doubleton variants (it means, there is only 'two' sample who having variant allele in a variant across final dataset) | gene.fail.lst | LIST | --genetest | --skato | A list of gene names that failed to perform SKAT-o test | filter.sample.lst | TSV | --incgeno --filgeno |
NONE | A list of sample filtering status by filtering criteria | allmiss.sample.lst | TSV | NONE | NONE | A list of samples having NO available genotype | linear.regr.res | TSV | --regression | --interaction | A result of regression analysis with continuous phenotype | logistic.regr.res | TSV | --regression | --interaction | A result of regression analysis with dichotomous phenotype | family.qls.res | TSV | --fqls | --mqls --avail --fqlsnopddt --retestthr |
A result of Family QLS analysis | estimated.maf | TSV | --freq corr | NONE | An estimated MAF from sample relatedness | all.maf | TSV | --freq all | NONE | A computed MAF using all samples | founders.maf | TSV | --freq founder | NONE | A computed MAF using only founder samples | power.single.res | TSV | --powercalc | NONE | A result of power calculation from single phenotype | power.multi.res | TSV | --powercalc | NONE | A result of power calculation from multiple phenotypes | miss.pheno.lst | TSV | NONE | --sampvar --pname |
A list of samples having phenotype missingness | miss.sex.lst | TSV | NONE | NONE | A list of samples having sex missingness | summary.gene.lst | TSV | --genetest --genesummary |
NONE | A summary of analyzed gene-variant information | summary.gmap.lst | TSV | --genetest --gmapsummary Single binary phenotype |
NONE | A summary of variant distribution across case-control samples for each gene mapping | entire.dist.dsg | TSV | --dsgdist | NONE | A distribution of dosage for entire dataset | sample.dist.dsg | TSV | --dsgdist | NONE | A sample-wise distribution of dosage | ibs.cor | matrix/TSV | --ibs | --cormat | A matrix/list of pairs that contains computed IBS | empi.cor | matrix/TSV | --makecor | --cormat | A matrix/list of pairs that contains computed empirical kinship coefficients | empi.med.cor | matrix/TSV | --makecor --medcor |
--cormat | A matrix/list of pairs that contains computed median of empirical kinship coefficients | theo.cor | matrix/TSV | --pddt | --cormat | A matrix/list of pairs that contains computed theoretical kinship coefficients based on the pedigree structure | hybrid.cor | matrix/TSV | --hybrid | --cormat | A matrix/list of pairs that contains mixed kinship coefficients | pearson.cor | matrix/TSV | --corpearson | --cormat | A matrix/list of pairs that contains Pearson's correlation coefficients | ktau.cor | matrix/TSV | --ktau | --cormat | A matrix/list of pairs that contains Kendall's tau correlation coefficients from raw genotype data | empi.ktau.cor | matrix/TSV | --empiktau | --cormat | A matrix/list of pairs that contains Kendall's tau correlation coefficients from normalized genotype data | ped | PLINK PED | --makeped | NONE | PED-formatted output of filtered dataset | map | PLINK MAP | --makeped --makelgen |
NONE | MAP-formatted output of filtered dataset, accompanied by ped(--makeped) or lgen(--makelgen) | tped | PLINK transposed PED | --maketped | NONE | Transposed PED-formatted output of filtered dataset | tfam | PLINK FAM | --maketped | NONE | FAM-formatted output of filtered dataset, accompanied by tped | lgen | Long-format dataset | --makelgen | NONE | Long-formatted output of filtered dataset | vcf | VCF | --makevcf | NONE | VCF output of filtered dataset | bed | PLINK binary PED | --makebed | NONE | BED-formatted output of filtered dataset | bim | PLINK FAM | --makebed | NONE | BIM-formatted output of filtered dataset, accompanied by bed | fam | PLINK FAM | --makevcf --makebed --makelgen |
NONE | FAM-formatted output of filtered dataset, accompanied by bed(--makebed) or lgen(--makelgen) | raw | PLINK RAW | --makeraw --makedom --makerec |
NONE | RAW-formatted output of filtered dataset, additive-coded genotype | structure.fam | ARBITRARY | --famsummary | NONE | A report of retrieved pedigree structure | structure.nucl.fam | ARBITRARY | --ncsummary | NONE | A report of retrieved pedigree structure by nuclear family | qtest.res | TSV | --qtest | NONE | A result of Q-test | gemma.res | TSV | --femma | NONE | A result of GEMMA | mdr.res | TSV | --mdr | NONE | A result of MDR | pca.res | TSV | --pca | --npc | A list of computed PC scores | density.variant.lst | TSV | --density | NONE | A result of physical variant density by window | scoretest.res | TSV | --scoretest | --lrt --pddt |
A result of Score test | covar.mat | TSV | --makecov | --sampvar --cname --baseline |
A matrix of covariates that actually used in the analyses, constructed from given covariates and final dataset | pheno.mat | TSV | --makepheno | --sampvar --pname |
A matrix of phenotype(s) that actually used in the analyses, constructed from given phenotypes and final dataset | poly.est.res | table | --heritability | --ml --specdcmp --aithr |
A result of heritability estimation | altcor.miss.lst | LIST | --cor | NONE | A list of sample IDs consists of the samples not included in the final dataset, but exists in the alternative correlation file | samplist.miss.lst | LIST | --remsamp/--selsamp | NONE | A list of sample IDs consists of the samples not included in the final dataset, but exists in the sample list file | stat.sample.lst | TSV | NONE | NONE | A report of samples about whether sample is included in the final dataset or not, and the reason of the sample was not included if it was not included | gen | GEN | --makegen | NONE | GEN-formatted output of filtered dataset | sample | SAMPLE | --makegen/--makebgen | NONE | Sample information of GEN-formatted output | bgen | Binary GEN | --makebgen | NONE | Binarized GEN-formatted output of filtered dataset | variant.lst | TSV | --listvariant | NONE | A list of variant IDs that actually included in the final dataset | sample.lst | TSV | --listsample | NONE | A list of sample IDs that actually included in the final dataset | founder.lst | TSV | --listfounder | NONE | A list of founder sample IDs that actually included in the final dataset | allelic.excl.lst | LIST | --vcf | NONE | A list of variant IDs of the variants excluded before an analysis due to it contains more than two alleles (triallelic or polyallelic) | set.gene.lst | LIST | --makeset | --settype | Gene-marker definition formatted set after mapping between original gene-marker definition and final dataset |
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