Description Usage Arguments Value Examples
compute mixture data given projection matrix (RNAseq)
1 2 3 4 5 6 7 | getx1.rnaseq(
NB0 = "top_bonferroni",
resultb0,
dge_s,
MAXITER = 1000,
x0 = NULL
)
|
NB0 |
number of genes to be retained, ordered by f-stat p-value. Other options: "all" uses all genes, "top_bonferroni" uses genes with adjusted p-values <0.05 after bonferroni correction, "top_fdr" uses genes with adjusted p-values <0.05 after FDR correction. Default is "top-bonferroni" |
resultb0 |
output of |
dge_s |
output of |
MAXITER |
integer number of iterations allowed |
x0 |
initial cell type composition for fitting |
x1 cell mixture of sample
converged convergence. 1=converged
1 2 3 4 5 6 7 | ## Not run:
data("data_celltypes_rnaseq")
dge.celltypes = getdge(cnts.celltypes, design.rnaseq, ncpm.min=1, nsamp.min=4)
b0 = getb0.rnaseq(dge.celltypes, design.rnaseq, ncpm.min=1, nsamp.min=4, sigg=NULL)
resultx1 = getx1.rnaseq(NB0="top_bonferroni",b0,dge.celltypes)
## End(Not run)
|
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