Description Usage Arguments Value
View source: R/preprocessing.R
Creation of a casper object.
1 2 3 4 5 6 | CreateCasperObject(raw.data, annotation, control.sample.ids, cytoband,
loh.name.mapping, cnv.scale, loh.scale, method, loh,
project = "casperProject", sequencing.type, expr.cutoff = 4.5,
display.progress = TRUE, log.transformed = TRUE,
centered.threshold = 3, window.length = 50, length.iterations = 50,
vis.bound = 2, noise.thr = 0.3, genomeVersion = "hg19", ...)
|
raw.data |
the matrix of genes (rows) vs. cells (columns) containing the raw counts |
annotation |
data.frame containing positions of each gene along each chromosome in the genome |
control.sample.ids |
vector containing the reference (normal) cell (sample) names |
cytoband |
cytoband information downloaded from UCSC hg19: http://hgdownload.cse.ucsc.edu/goldenpath/hg19/database/cytoBand.txt.gz hg38:http://hgdownload.cse.ucsc.edu/goldenpath/hg38/database/cytoBand.txt.gz |
loh.name.mapping |
contains the cell (sample) name and the matching baf signal sample name |
cnv.scale |
maximum expression scale |
loh.scale |
maximum baf scale |
method |
analysis type: itereative or fixed (default: iterative) |
loh |
The original baf signal |
sequencing.type |
sequencing.type sequencing type: bulk or single-cell |
expr.cutoff |
expression cutoff for lowly expressed genes |
log.transformed |
indicates if the data log2 transformed or not. (default:TRUE) |
centered.threshold |
|
window.length |
window length used for median filtering (default: 50) |
length.iterations |
increase in window length at each scale iteration (default: 50) |
vis.bound |
threshold for control normalized data for better visualization (default: 2) |
genomeVersion |
genomeVersion: hg19 or hg38 (default: hg19) |
casper
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