calculateDiffMeth | R Documentation |
The function calculates differential methylation statistics between two groups of samples. The function uses either logistic regression test or Fisher's Exact test to calculate differential methylation. See the rest of the help page and references for detailed explanation on statistics.
calculateDiffMeth(
.Object,
covariates = NULL,
overdispersion = c("none", "MN", "shrinkMN"),
adjust = c("SLIM", "holm", "hochberg", "hommel", "bonferroni", "BH", "BY", "fdr",
"none", "qvalue"),
effect = c("wmean", "mean", "predicted"),
parShrinkMN = list(),
test = c("F", "Chisq", "fast.fisher", "midPval"),
mc.cores = 1,
slim = TRUE,
weighted.mean = TRUE,
chunk.size = 1e+06,
save.db = FALSE,
...
)
## S4 method for signature 'methylBaseDB'
calculateDiffMeth(
.Object,
covariates = NULL,
overdispersion = c("none", "MN", "shrinkMN"),
adjust = c("SLIM", "holm", "hochberg", "hommel", "bonferroni", "BH", "BY", "fdr",
"none", "qvalue"),
effect = c("wmean", "mean", "predicted"),
parShrinkMN = list(),
test = c("F", "Chisq", "fast.fisher", "midPval"),
mc.cores = 1,
slim = TRUE,
weighted.mean = TRUE,
chunk.size = 1e+06,
save.db = TRUE,
...
)
.Object |
a |
covariates |
a |
overdispersion |
If set to "none"(default), no overdispersion correction will be attempted. If set to "MN", basic overdispersion correction, proposed by McCullagh and Nelder (1989) will be applied.This correction applies a scaling parameter to variance estimated by the model. EXPERIMENTAL: If set to "shrinkMN", scaling parameter will be shrunk towards a common value (not thoroughly tested as of yet). |
adjust |
different methods to correct the p-values for multiple testing.
Default is "SLIM" from methylKit. For "qvalue" please see
|
effect |
method to calculate the mean methylation different between groups using read coverage as weights (default). When set to "mean", the generic mean is applied and when set to "predicted", predicted means from the logistic regression model is used for calculating the effect. |
parShrinkMN |
a list for squeezeVar(). (NOT IMPLEMENTED) |
test |
the statistical test used to determine the methylation differences. The Chisq-test is used by default for more than two groups, while the F-test can be chosen if overdispersion control is applied. If there is one sample per group the Fisher's exact test will be applied using "fast.fisher", while "midPval" can be choosen to boost calculation speed. See details section for more information. |
mc.cores |
integer denoting how many cores should be used for parallel differential methylation calculations (can only be used in machines with multiple cores). |
slim |
If set to FALSE, |
weighted.mean |
If set to FALSE, |
chunk.size |
Number of rows to be taken as a chunk for processing the
|
save.db |
A Logical to decide whether the resulting object should be saved as flat file database or not, default: explained in Details section. |
... |
optional Arguments used when save.db is TRUE
|
a methylDiff
object containing the differential methylation
statistics and locations for regions or bases
Covariates can be included in the analysis. The function will then try to
separate the
influence of the covariates from the treatment effect via a linear model.
The Chisq-test is used per default only when no overdispersion correction is
applied.
If overdispersion correction is applied, the function automatically switches
to the
F-test. The Chisq-test can be manually chosen in this case as well, but the
F-test only
works with overdispersion correction switched on.
If there is one sample in each group, e.g. after applying the pooling samples,
the Fisher's exact test will be applied for differential methylation.
methyKit offers two implementations to perform this test, which yield
slightly different results but differ much in computation time.
"fast.fisher" is a cut down version 'fisher.test()' that should produce
the exact same results as the base implementation, while "midPval"
will produce marginaly different p-values, but offers a large boost in
calculation speed.
The parameter chunk.size
is only used when working with
methylBaseDB
objects, as they are read in chunk by chunk to enable
processing large-sized objects which are stored as flat file database.
Per default the chunk.size is set to 1M rows, which should work for most systems.
If you encounter memory problems or
have a high amount of memory available feel free to adjust the chunk.size
.
The parameter save.db
is per default TRUE for
methylDB objects as methylBaseDB
,
while being per default FALSE for methylBase
.
If you wish to save the result of an
in-memory-calculation as flat file database or if the size of the database
allows the calculation in-memory,
then you might want to change the value of this parameter.
Altuna Akalin, Matthias Kormaksson, Sheng Li, Francine E. Garrett-Bakelman, Maria E. Figueroa, Ari Melnick, Christopher E. Mason. (2012). "methylKit: A comprehensive R package for the analysis of genome-wide DNA methylation profiles." Genome Biology.
McCullagh and Nelder. (1989). Generalized Linear Models. Chapman and Hall. London New York.
Barnard. (1989). On alleged gains in power from lower P-values. Statistics in Medicine. Armitage and Berry. (1994) Statistical Methods in Medical Research (3rd edition). Blackwell.
pool
, reorganize
dataSim
data(methylKit)
# The Chisq-test will be applied when no overdispersion control is chosen.
my.diffMeth=calculateDiffMeth(methylBase.obj,covariates=NULL,
overdispersion=c("none"),
adjust=c("SLIM"))
# pool samples in each group
pooled.methylBase=pool(methylBase.obj,sample.ids=c("test","control"))
# After applying the pool() function, there is one sample in each group.
# The Fisher's exact test will be applied for differential methylation.
my.diffMeth2=calculateDiffMeth(pooled.methylBase,covariates=NULL,
overdispersion=c("none"),
adjust=c("SLIM"))
# Covariates and overdispersion control:
# generate a methylBase object with age as a covariate
covariates=data.frame(age=c(30,80,30,80))
sim.methylBase<-dataSim(replicates=4,sites=1000,treatment=c(1,1,0,0),
covariates=covariates,
sample.ids=c("test1","test2","ctrl1","ctrl2"))
# Apply overdispersion correction and include covariates
# in differential methylation calculations.
my.diffMeth3<-calculateDiffMeth(sim.methylBase,
covariates=covariates,
overdispersion="MN",test="Chisq",mc.cores=1)
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