Files in tstokowy/RareVariantVis
A suite for analysis of rare genomic variants in whole genome sequencing data
.Rbuildignore
DESCRIPTION
NAMESPACE
R/callHomozygous.R
R/chromosomeVis.R
R/getCrisprGuides.R
R/movingAverage.R
R/multipleVis.R
R/rareVariantVis.R
RareVariantVis.Rproj
inst/CITATION
inst/extdata/All_20160601_chr19_9-10.vcf.recode.vcf.gz
inst/extdata/All_20160601_chr19_9-10.vcf.recode.vcf.gz.tbi
inst/extdata/CentromeresHg19.txt
inst/extdata/CoriellIndex_S1.sv.vcf.gz
inst/extdata/CoriellIndex_S1.sv.vcf.gz.tbi
inst/extdata/CoriellIndex_S1_chr19_9-10_S1.vcf.recode.vcf.gz
inst/extdata/CoriellIndex_S1_chr19_9-10_S1.vcf.recode.vcf.gz.tbi
inst/extdata/ExAC.r0.3.1.sites.vep_chr19_9-10.vcf.recode.vcf.gz
inst/extdata/ExAC.r0.3.1.sites.vep_chr19_9-10.vcf.recode.vcf.gz.tbi
inst/extdata/RareVariants_CoriellIndex_S1.txt
inst/extdata/RareVariants_Coriell_S2.txt
inst/extdata/RareVariants_Coriell_S3.txt
inst/extdata/StructuralVariants_CoriellIndex_S1.txt
inst/extdata/StructuralVariants_Coriell_S2.txt
inst/extdata/StructuralVariants_Coriell_S3.txt
inst/extdata/UCSC_hg19_chr9_9-10_refSeq_160702.txt
inst/extdata/nexterarapidcapture_exome_targetedregions_v1.2_chr19_9-10.bed
inst/extdata/uniprot-all_chr19_9-10.txt
man/.Rapp.history
man/callHomozygous.Rd
man/chromosomeVis.Rd
man/getCrisprGuides.Rd
man/movingAverage.Rd
man/multipleVis.Rd
man/rareVariantVis.Rd
vignettes/CoriellIndex_S1_chr19.png
vignettes/RareVariantsVis.Rnw
vignettes/interactive.png
