lfcShrink {DESeq2} | R Documentation

## Shrink log2 fold changes

### Description

Adds shrunken log2 fold changes (LFC) and SE to a results table from `DESeq` run without LFC shrinkage. Three shrinkage esimators for LFC are available via `type`.

### Usage

    lfcShrink(dds, coef, contrast, res, type = c("normal", "apeglm", "ashr"),
      lfcThreshold = 0, svalue = FALSE, returnList = FALSE, apeAdapt = TRUE,
      apeMethod = "nbinomCR", parallel = FALSE, BPPARAM = bpparam(),
      quiet = FALSE, ...)

### Arguments

`dds` | a DESeqDataSet object, after running `DESeq`
`coef` | the name or number of the coefficient (LFC) to shrink, consult `resultsNames(dds)` after running `DESeq(dds)`. note: only `coef` or `contrast` can be specified, not both. `apeglm` requires use of `coef`.
`contrast` | see argument description in `results`. only `coef` or `contrast` can be specified, not both.
`res` | a DESeqResults object. Results table produced by the default pipeline, i.e. `DESeq` followed by `results`. If not provided, it will be generated internally using `coef` or `contrast`. For `ashr`, if `res` is provided, then `coef` and `contrast` are ignored.
`type` | `"normal"` is the original DESeq2 shrinkage estimator; `"apeglm"` is the adaptive t prior shrinkage estimator from the 'apeglm' package; `"ashr"` is the adaptive shrinkage estimator from the 'ashr' package, using a fitted mixture of normals prior - see the Stephens (2016) reference below for citation
`lfcThreshold` | a non-negative value which specifies a log2 fold change threshold (as in `results`). This can be used in conjunction with `normal` and `apeglm`, where it will produce new p-values or s-values testing whether the LFC is greater in absolute value than the threshold. The s-values returned in combination with `apeglm` provide the probability of FSOS events, "false sign or small", among the tests with equal or smaller s-value than a given gene's s-value, where "small" is specified by `lfcThreshold`.
`svalue` | logical, should p-values and adjusted p-values be replaced with s-values when using `apeglm` or `ashr`. s-values provide the probability of false signs among the tests with equal or smaller s-value than a given given's s-value. See Stephens (2016) reference on s-values.
`returnList` | logical, should `lfcShrink` return a list, where the first element is the results table, and the second element is the output of `apeglm` or `ashr`
`apeAdapt` | logical, should `apeglm` use the MLE estimates of LFC to adapt the prior, or use default or specified `prior.control`
`apeMethod` | what `method` to run `apeglm`, which can differ in terms of speed
`parallel` | if FALSE, no parallelization. if TRUE, parallel execution using `BiocParallel`, see same argument of `DESeq` parallelization only used with `normal` or `apeglm`
`BPPARAM` | see same argument of `DESeq`
`quiet` | whether to print messages
`...` | arguments passed to `apeglm` and `ashr`

### Details

As of DESeq2 version 1.18, `type="apeglm"` and `type="ashr"` are new features, and still under development. Specifying `apeglm` passes along DESeq2 MLE log2 fold changes and standard errors to the `apeglm` function in the apeglm package, and re-estimates posterior LFCs for the coefficient specified by `coef`. Specifying `ashr` passes along DESeq2 MLE log2 fold changes and standard errors to the `ash` function in the ashr package, with arguments `mixcompdist="normal"` and `method="shrink"`. See vignette for a comparison of shrinkage estimators on an example dataset. For all shrinkage methods, details on the prior is included in `priorInfo(res)`, including the `fitted_g` mixture for ashr. The integration of shrinkage methods from external packages will likely evolve over time. We will likely incorporate an `lfcThreshold` argument which can be passed to apeglm to specify regions of the posterior at an arbitrary threshold.

For `normal`, and design as a formula, shrinkage cannot be applied to coefficients in a model with interaction terms. For `normal` and user-supplied model matrices, shrinkage is only supported via `coef`. For `normal` with numeric- or list-style contrasts, it is possible to use `lfcShrink`, but likely easier to use `DESeq` with `betaPrior=TRUE` followed by `results`, because the numeric or list should reference the coefficients from the expanded model matrix. These coefficients will be printed to console if 'contrast' is used with `normal`.

### Value

a DESeqResults object with the `log2FoldChange` and `lfcSE` columns replaced with shrunken LFC and SE. `priorInfo(res)` contains information about the shrinkage procedure, relevant to the various methods specified by `type`.

### References

`type="normal"`:

Love, M.I., Huber, W., Anders, S. (2014) Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biology, 15:550. https://doi.org/10.1186/s13059-014-0550-8

`type="apeglm"`:

Zhu, A., Ibrahim, J.G., Love, M.I. (2018) Heavy-tailed prior distributions for sequence count data: removing the noise and preserving large differences. bioRxiv. https://doi.org/10.1101/303255

`type="ashr"`:

Stephens, M. (2016) False discovery rates: a new deal. Biostatistics, 18:2. https://doi.org/10.1093/biostatistics/kxw041

### Examples

    set.seed(1)
    dds <- makeExampleDESeqDataSet(n=500,betaSD=1)
    dds <- DESeq(dds)
    res <- results(dds)

    # these are the coefficients from the model
    # we can specify them using 'coef' by name or number below
    resultsNames(dds)

    res.shr <- lfcShrink(dds=dds, coef=2)
    res.shr <- lfcShrink(dds=dds, contrast=c("condition","B","A"))
    res.ape <- lfcShrink(dds=dds, coef=2, type="apeglm")
    res.ash <- lfcShrink(dds=dds, coef=2, type="ashr")

[Package DESeq2 version 1.20.0 Index]