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