DBAmmd Class defines a container for differential binding analysis
using MMDiff2. For this class a number of methods is foreseen, among which
accessors for every slot.
As MetaData, it needs to contain the path to the data directory and the
name of a sampleSheet csv file.
DBAmmd()returns an empty DBAmmd Object.
DBAmmd(MetaData) initializes a DBAmmd Object for a new
(See below and the package vignette for more details.)
List containing an
ExpData and an
AnaData compartment. "ExpData" needs a
dataDir and a
SampleSheet entry. A
genome entry, which should be a valid
BSGenome name, is useful to find sequence motifs. (Note the genome
version needs to correspond to the one used for the read alignment.
available.genomes() to find the right name.) The
entry is used to store and access parameters for the MMDiff2 Analysis, like the sigma
of the RBF Kernel.
GRanges object containing Regions of Interests (Peaks)
List containing positions of mapped reads, i.e. exact
start and end positions of mapped fragments. In the case of
single-end reads, the left most postions of fragments mapping to the positive
strands and the right most positions of fragments
mapping to the negative strands are stored in "Left.p" and "Right.n".
getPeakReads to fill this slot and
to add the (estimated) positions of fragment centers.
m x n matrix containing total counts of reads mapping to m peaks in n samples (including input samples)
m x n matrix containing counts of reads mapping to positive (forward) strand
m x n matrix containing counts of reads mapping to negative (reverse) strand
List of lists, each of length m (number of Peaks).
Compartments could be 'Left.p','Right.n','Left.n','Right.p','Center.n',
'Center.p','Center','Left','Right', defining whether left or right ends or
centers of fragments should be considered for positive ('p') or negative ('n')
strand, or both strands combined. For a given compartment there is one entry per
peak, which is a n x L_i matrix, where n is the number of samples and L_i is
the number of bins used to cover the extend of the peak. Note, L_i varies
between peaks of different lengths. See
compHists() for more details.
List with compartments for different methods to compute
distances (e.g. MMD). Each compartment contains a m x N matrix with computed
distances for each Peak between N pairs of samples.
compDists() for more details.
(for internal use only)
List of lists. Each entry contains a contrast i.e. the definition of two groups that should be compared to each other in a differential analysis. A Contrast needs entries "name1", "name2" for group names, as well as group memberships given in "group1" and "group2". Results of a differential test for this contrast are stored in an entry given by the method name, e.g. "MMD.locfit"
1 2 3 4 5 6 7 8 9 10
## Example using a small data set provided in the MMDiffBamSubset package # setting the Experiment meta data: ExpData <- list(dataDir=system.file("extdata", package="MMDiffBamSubset"), sampleSheet="Cfp1.csv") MetaData <- list('ExpData' = ExpData) # Creating a DBAmmd data set: MMD <- DBAmmd(MetaData)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.