adjustedCADD.annotation | SNVs and Indels annotation with adjusted CADD scores |
adjustedCADD.annotation.indels | Indels annotation with adjusted CADD scores |
adjustedCADD.annotation.SNVs | SNVs annotation with adjusted CADD scores |
bed.matrix.split.genomic.region | Bed matrix for variants associated to multiple genomic regions |
burden | Linear, logistic or multinomial regression on a genetic score |
burden.continuous | Linear regression on a genetic score |
burden.continuous.subscores | Linear regression on a multiple genetic scores within a genomic region |
burden.mlogit | Logistic or multinomial regression on a genetic score |
burden.mlogit.subscores | Logistic or multinomial regression on a multiple genetic scores within a genomic region |
burden.subscores | Linear, logistic or multinomial regression on a multiple genetic scores within a genomic region |
burden.weighted.matrix | Score matrix for burden tests |
CAST | Cohort Allelic Sum Test |
filter.adjustedCADD | Variant filtering based on frequency and median adjusted CADD by CADD regions |
filter.rare.variants | Rare variants filtering |
genes.b37 | Genes positions |
genes.b38 | Genes positions |
genes.positions | Genes positions |
genotypic.freq | Genotypic frequencies calculation for data simulations |
GnomADgenes | GnomADgenes dataset |
GRR.matrix | GRR matrix for genetic data simulation |
Jaccard | Jaccard index |
Kryukov | Kryukov data set |
LCT.hap | LCT haplotypes data set |
LCT.haplotypes | LCT haplotypes data set |
LCT.matrix | LCT genotypes matrix |
LCT.matrix.bed | LCT genotypes matrix |
LCT.matrix.fam | LCT genotypes matrix |
LCT.matrix.pop1000G | LCT genotypes matrix |
LCT.sample | LCT haplotypes data set |
LCT.snps | LCT haplotypes data set |
multinomial.asso.freq | Single variant association test with categorical phenotype |
NullObject.parameters | Null Model for SKAT and burden tests |
RAVA.FIRST | RAVA-FIRST: RAre Variant Association using Functionally-InfoRmed STeps |
rbm.GRR | Simulation of genetic data using GRR values |
rbm.GRR.power | Power of RVAT based on simulations and theoretical calculations (CAST) with GRR |
rbm.haplos.freqs | Simulation of genetic data based on haplotypic frequencies |
rbm.haplos.power | Power of RVAT based on simulations with haplotypes |
rbm.haplos.thresholds | Simulation of genetic data based on haplotypes and a libaility model |
set.CADDregions | Variants annotation based on 'CADD regions' and genomic categories |
set.genomic.region | Variants annotation based on gene positions |
set.genomic.region.subregion | Variants annotation based on regions and subregions positions |
SKAT | SKAT test |
SKAT.bootstrap | Multi group SKAT test using bootstrap sampling |
SKAT.continuous | Multi group SKAT test using Liu et al. approximation |
SKAT.permutations | Multi group SKAT test using bootstrap sampling |
SKAT.theoretical | Multi group SKAT test using Liu et al. approximation |
subregions.LCT | Exemple of functional categories |
WSS | WSS genetic score |