| norm.fact | R Documentation | 
This function calculates the normalization factor for each sample using different methods. See details.
norm.fact(
  df,
  method = c("TMM", "TMMex", "MedR", "QN"),
  logratioTrim = 0.3,
  sumTrim = 0.05,
  Weighting = TRUE,
  Acutoff = -1e+10
)
| df | a data frame or matrix of allele depth values (total depth per snp per sample) | 
| method | character. method to be used (see details). Default  | 
| logratioTrim | numeric. percentage value (0 - 1) of variation to be trimmed in log transformation | 
| sumTrim | numeric. amount of trim to use on the combined absolute
levels (“A” values) for method  | 
| Weighting | logical, whether to compute (asymptotic binomial precision) weights | 
| Acutoff | numeric, cutoff on “A” values to use before trimming | 
Originally described for normalization of RNA sequences
(Robinson & Oshlack 2010), this function computes normalization (scaling)
factors to convert observed library sizes into effective library sizes.
It uses the method trimmed means of M-values proposed by Robinson &
Oshlack (2010). See the original publication and edgeR package
for more information.
The method MedR is median ratio normalization;
QN - quantile normalization (see  Maza, Elie, et al. 2013 for a
comparison of methods).
Returns a numerical vector of normalization factors for each sample
Piyal Karunarathne
Robinson MD, and Oshlack A (2010). A scaling normalization method for differential expression analysis of RNA-seq data. Genome Biology 11, R25
Robinson MD, McCarthy DJ and Smyth GK (2010). edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26
## Not run: vcf.file.path <- paste0(path.package("rCNV"), "/example.raw.vcf.gz")
vcf <- readVCF(vcf.file.path)
df<-hetTgen(vcf,"AD-tot",verbose=FALSE)
norm.fact(df)
## End(Not run)
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