WISARD[wɪzərd]
Workbench for Integrated Superfast Association study with Related Data
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Detail of [all.hwe]

  • A computed HWE using all samples
  • Output format is TSV
    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

    Output Index

    Here is the list of all outputs produced from WISARD.
    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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    Last modified : 2022-09-08 17:16:37