Description Usage Arguments Value Note
A function to gather information about a given gene list
that will be needed to fit the background mutation model.
It pulls out the sequence of the genes in the list
X
, as well as indicates which of the positions
resides in a CpG dinucleotide pair, and counts how many
base pairs are at risk for mutation in the 108
combinations of 6 mutation types x 2 silent/nonsilent
status x 3 replication timing categories x 3 expression
level categories.
1 | preprocess.BM(X, gene)
|
X |
a list with one entry for each chromosome, where
each entry is a matrix containing a row for each coding
base pair and the following columns: 1. base pair
position, 2. nucleotide number (see
|
gene |
a list with one entry for each gene, each entry is another list of 5 elements: Ensembl name, chromosome, base pairs, replication timing region (1=Early, 2=Middle, 3=Late), and expression level (1=Low, 2=Medium, 3=High). |
a list with three items:
seq.in.chrom |
a list with an item for each chromosome that contains a matrix whose first column is the position and the second column is the nucleotide of a base pair within that chromosomes |
dCG.in.chrom |
position of the CpG dinucleotide coding sequences within chromosomes |
type.const |
a 3 by 12 matrix containing E_1,n,h,F_2,n,h,E_3,n,h,F_4,n,h,E_5,n,h,F_6,n,h, C_1,n,h,D_2,n,h,C_3,n,h,D_4,n,h,C_5,n,h,D_6,n,h for n=1,2,3, and h=1,2,3 |
This internal function is not intended to be called by the user.
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