Description Usage Arguments Details Value Note Author(s) References See Also
Identify which genes are significantly differentially expressed for each contrast from a fit object containing p-values and test statistics. A number of different multiple testing strategies are offered that adjust for multiple testing down the genes as well as across contrasts for each gene.
1 2 3 4 5 6 7 | ## S3 method for class 'MArrayLM'
decideTests(object, method = "separate", adjust.method = "BH", p.value = 0.05,
lfc = 0, ...)
## Default S3 method:
decideTests(object, method = "separate", adjust.method = "BH", p.value = 0.05,
lfc = 0, coefficients = NULL, cor.matrix = NULL, tstat = NULL, df = Inf,
genewise.p.value = NULL, ...)
|
object |
a numeric matrix of p-values or an |
method |
character string specifying how genes and contrasts are to be combined in the multiple testing scheme. Choices are |
adjust.method |
character string specifying p-value adjustment method. Possible values are |
p.value |
numeric value between 0 and 1 giving the required family-wise error rate or false discovery rate. |
lfc |
numeric, minimum absolute log2-fold-change required. |
coefficients |
numeric matrix of coefficients or log2-fold-changes. Of same dimensions as |
cor.matrix |
correlation matrix of coefficients. Square matrix of dimension |
tstat |
numeric matrix of t-statistics. Of same dimensions as |
df |
numeric vector of length |
genewise.p.value |
numeric vector of length |
... |
other arguments are not used. |
This function can be applied to a matrix of p-values but is more often applied to an MArrayLM
fit object produced by eBayes
or treat
.
In either case, rows of object
correspond to genes and columns to coefficients or contrasts.
This function applies a multiple testing procedure and a significance level cutoff to the statistics contained in object
.
It implements a number of multiple testing procedures for determining whether each statistic should be considered significantly different from zero.
method="separate"
will apply multiple testing adjustments to each column of p-values separately.
Setting method="separate"
is equivalent to using topTable
separately for each coefficient in the linear model fit and will identify the same probes as significantly differentially expressed if adjust.method
is the same.
method="global"
will treat the entire matrix of t-statistics as a single vector of unrelated tests.
method="hierarchical"
adjusts down genes and then across contrasts.
method="nestedF"
adjusts down genes according to overall F-tests and then uses classifyTestsF
to classify contrasts as significant or not for the selected genes.
The default method="separate"
and adjust.method="BH"
settings are appropriate for most analyses.
method="global"
is useful when it is important that the same t-statistic cutoff should correspond to statistical significance for all the contrasts.
The "nestedF"
method was proposed by Michaud et al (2008) and achieves better consistency between contrasts than the other methods.
It provides formal error rate control at the gene level but not for individual contrasts.
See the classifyTestsF
help page for more detail about the "nestedF"
method.
If object
is a MArrayLM linear model fit, then the "hierarchical"
method conducts row-wise F-tests and then proceeds to t-tests for those rows with significant F-tests.
The multiple testing adjustment is applied initially to the F-tests and then, with an adjusted level, to the t-tests for each significant row.
Also see the limma User's Guide for a discussion of the statistical properties of the various adjustment methods.
An object of class TestResults
.
This is essentially a numeric matrix with elements -1
, 0
or 1
depending on whether each t-statistic is classified as significantly negative, not significant or significantly positive.
If lfc>0
then contrasts are judged significant only when the log2-fold change is at least this large in absolute value.
For example, one might choose lfc=log2(1.5)
to restrict to 50% changes or lfc=1
for 2-fold changes.
In this case, contrasts must satisfy both the p-value and the fold-change cutoff to be judged significant.
Although this function enables users to set p-value and lfc cutoffs simultaneously, this combination criterion is not generally recommended.
Unless the fold changes and p-values are very highly correlated, the addition of a fold change cutoff can increase the family-wise error rate or false discovery rate above the nominal level.
Users wanting to use fold change thresholding are recommended to use treat
instead of eBayes
and to leave lfc
at the default value when using decideTests
.
Gordon Smyth
Michaud, J, Simpson, KM, Escher, R, Buchet-Poyau, K, Beissbarth, T, Carmichael, C, Ritchie, ME, Schutz, F, Cannon, P, Liu, M, Shen, X, Ito, Y, Raskind, WH, Horwitz, MS, Osato, M, Turner, DR, Speed, TP, Kavallaris, M, Smyth, GK, and Scott, HS (2008). Integrative analysis of RUNX1 downstream pathways and target genes. BMC Genomics 9, 363.
An overview of multiple testing functions is given in 08.Tests.
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