chrnames: Pull out the chromosome names from a cross

GITHUB
byandell/qtl: Tools for analyzing QTL experiments

Description
Pull out the chromosome names from a cross object as one big vector.
Usage

chrnames: Extract chromosome names

GITHUB
neyhartj/pbsim: Simulations of Plant Breeding Experiments

chromosome names
Usage
chrnames(genome)

chrnames: Pull out the chromosome names from a cross

GITHUB
kbroman/qtl: Tools for Analyzing QTL Experiments

a cross
Description
Pull out the chromosome names from a cross object as one big vector.

chrnames: Pull out the chromosome names from a cross

CRAN
qtl: Tools for Analyzing QTL Experiments

a cross
Description
Pull out the chromosome names from a cross object as one big vector.

chrNames: Retrieve chromosome names from an object

BIOC
ChromHeatMap: Heat map plotting by genome coordinate

chromosome.
Usage
chrNames(object)

chrnames: Extract chromosome names

GITHUB
neyhartj/qgsim: Simulations of Plant Breeding Experiments

chromosome names
Usage
chrnames(genome)

chrNames-methods: Get list of unique chromosome names

BIOC
genoset: A RangedSummarizedExperiment with methods for copy number analysis

list of unique chromosome names
Usage
chrNames(object)

chrNames-methods: Chromosome names method for ranged objects

CRAN
humarray: Simplify Analysis and Annotation of Human Microarray Datasets

R: Chromosome names method for ranged objects
chrNames,RangedData-methodR Documentation
Chromosome names method

tests/testthat/test:

GITHUB
Yuewei-Wang/nsSNPfinder: nsSNP Postion Finder and Visualization

arguments in chromosome 1", {
chrName = 3
startPosition = 49359145

tests/testthat/test-nsSNPFreqPlot.R:

GITHUB
Yuewei-Wang/nsSNPfinder: nsSNP Postion Finder and Visualization

(nsSNPfinder)
test_that("invalid input1: wrong chromosome name", {
chrName = 30

tests/testthat/test-SNPFreqPlot.R:

GITHUB
Yuewei-Wang/nsSNPfinder: nsSNP Postion Finder and Visualization

(nsSNPfinder)
test_that("invalid input1: wrong chromosome name", {
chrName = 25

R/fixChromosomeNames.R:

GITHUB
MHi-C/MHiC: MHiC

fixChromosomeNames <- function(chrnames)
#capital to small
chrnames <- paste0("chr", chrnames)

R/fixChromosomeNames.R:

GITHUB
Skhakmardan/MHiC: MHiC

fixChromosomeNames <- function(chrnames)
#capital to small
chrnames <- paste0("chr", chrnames)

R/GTFnomencJunctionM.R:

GITHUB
harshsharma-cb/FASE: Analysis of RNA-Sequencing data using FASE (Finding Alternative Splicing Events).

chrnames<- strsplit(needtochanges[indexTochange],'chr')
chrnames<- unlist(lapply(chrnames, function(x) x[2]))
needtochanges

tests/testthat/test-displayPDB.R:

GITHUB
Yuewei-Wang/nsSNPfinder: nsSNP Postion Finder and Visualization

test_that("invalid input1: incorrect chromosome name", {
chrName = 'r'
geneName = 'RHOA'

R/snpinfo.R:

GITHUB
DavisBrian/seqMetaPipeline:

, snpNames=NULL, aggregateBy=NULL, filterBy=NULL, chrName=NULL) {
if (is.null(snpNames) & is.null(aggregateBy

R/citrusSize.R:

CRAN
idiogramFISH: Shiny App. Idiograms with Marks and Karyotype Indices

mark (markOverCMA)
#' @param chrName character, defaults to "B", chr. name(s) to duplicate mark (markOverCMA)
#' @param

R/perMark.R:

CRAN
idiogramFISH: Shiny App. Idiograms with Marks and Karyotype Indices

(listOfdfChromSize)[i]
dup_chr <- any(duplicated(listOfdfChromSize[[i]]$chrName))
if (dup_chr == FALSE

R/SeqData-helperFunctions.R:

GITHUB
sheng-liu/SeqData: A data structure and four simple tools build upon it for sequencing data analysis

names into standard UCSC naming convention "chrX"
.checkChrNames=function(chrNames){
# convert names to character