Man pages for JH-Zhou/HandyCNV
HandyCNV: An R package for Standardized Summary, Annotation, Comparison, and Visualization of CNV, CNVR and ROH

call_cnvrGenerate CNV Regions (CNVR)
call_geneAnnotate gene for intervals (CNV, CNVR, ROH or QTL)
clean_ensgeneClean Ensembl reference gene list
clean_ucscClean USCS reference gene list
closer_snpPick out the names and positions of start and end SNPs of a...
cnv_cleanClean CNV
cnvr_plotCustom CNVR distribution map and plot all high frequency CNVR...
cnv_summary_plotSummary plots for CNVs
cnv_visualCustom visualizing CNV
compare_cnvCompare CNV
compare_cnvrCompare CNVR
compare_geneFind the consensus genes by comparing the frequency of gene...
compare_intervalTitle compare_interval compare cnvr, each input file should...
convert_coordConvert coordinates of genomic intervals
convert_mapConvert map file
get_demoGet demo data
get_haplotypeGet haplotype
get_refgeneGet reference gene
get_samplesTitle get_samples
haplo_visualThe order of haplotype present in plot are start from high...
plot_cnvr_panoramaPlotting CNVR with all relevant information
plot_cnvr_sourcePlotting CNVs by the source information
plot_geneCustom plotting gene from reference gene list
plot_snp_densityTitle SNP density plot
prep_phasedPrepare the phased genotype into the standard format
roh_visualCustom Visualizing ROH
roh_windowSliding window to capture the high frequent ROH region
JH-Zhou/HandyCNV documentation built on Dec. 18, 2021, 12:25 a.m.