allFitnessEffects {OncoSimulR} | R Documentation

## Create fitness and mutation effects specification from restrictions, epistasis, and order effects.

### Description

Given one or more of a set of poset restrictions, epistatic interactions, order effects, and genes without interactions, as well as, optionally, a mapping of genes to modules, return the complete fitness specification.

For mutator effects, given one or more of a set of epistatic interactions and genes without interactions, as well as, optionally, a mapping of genes to modules, return the complete specification of how mutations affect the mutation rate.

The output of these functions is not intended for user consumption, but as a way of preparing data to be sent to the C++ code.

### Usage

    allFitnessEffects(rT = NULL, epistasis = NULL, orderEffects = NULL,
      noIntGenes = NULL, geneToModule = NULL, drvNames = NULL,
      genotFitness = NULL,  keepInput = TRUE)

    allMutatorEffects(epistasis = NULL, noIntGenes = NULL,
                       geneToModule = NULL,
                      keepInput =  TRUE)

### Arguments

`rT` | A restriction table that is an extended version of a poset (see `poset` ). A restriction table is a data frame where each row shows one edge between a parent and a child. A restriction table contains exactly these columns, in this order: parent The identifiers of the parent nodes, in a parent-child relationship. There must be at least on entry with the name "Root". child The identifiers of the child nodes. s A numeric vector with the fitness effect that applies if the relationship is satisfied. sh A numeric vector with the fitness effect that applies if the relationship is not satisfied. This provides a way of explicitly modeling deviatons from the restrictions in the graph, and is discussed in Diaz-Uriarte, 2015. typeDep The type of dependency. Three possible types of relationship exist: AND, monotonic, or CMPN Like in the CBN model, all parent nodes must be present for a relationship to be satisfied. Specify it as "AND" or "MN" or "monotone". OR, semimonotonic, or DMPN A single parent node is enough for a relationship to be satisfied. Specify it as "OR" or "SM" or "semimonotone". XOR or XMPN Exactly one parent node must be mutated for a relationship to be satisfied. Specify it as "XOR" or "xmpn" or "XMPN". In addition, for the nodes that depend only on the root node, you can use "–" or "-" if you want (though using any of the other three would have the same effects if a node that connects to root only connects to root).
`epistasis` | A named numeric vector. The names identify the relationship, and the numeric value is the fitness (or mutator) effect. For the names, each of the genes or modules involved is separated by a ":". A negative sign denotes the absence of that term.
`orderEffects` | A named numeric vector, as for `epistasis`. A ">" separates the names of the genes of modules of a relationship, so that "U > Z" means that the relationship is satisfied when mutation U has happened before mutation Z.
`noIntGenes` | A numeric vector (optionally named) with the fitness coefficients (or mutator multiplier factor) of genes (only genes, not modules) that show no interactions. These genes cannot be part of modules. But you can specify modules that have no epistatic interactions. See examples and vignette. Of course, avoid using potentially confusing characters in the names. In particular, "," and ">" are not allowed as gene names.
`geneToModule` | A named character vector that allows to match genes and modules. The names are the modules, and each of the values is a character vector with the gene names, separated by a comma, that correspond to a module. Note that modules cannot share genes. There is no need for modules to contain more than one gene. If you specify a geneToModule argument, and you used a restriction table, the `geneToModule` must necessarily contain, in the first position, "Root" (since the restriction table contains a node named "Root"). See examples below.
`drvNames` | The names of genes that are considered drivers. This is only used for: a) deciding when to stop the simulations, in case you use number of drivers as a simulation stopping criterion (see `oncoSimulIndiv`); b) for summarization purposes (e.g., how many drivers are mutated); c) in figures. But you need not specifiy anything if you do not want to, and you can pass an empty vector (as `character(0)`). The default has changed with respect to v.2.1.3 and previous: it used to be to assume that all genes that were not in the `noIntGenes` were drivers. The default now is to assume nothing: if you want `drvNames` you have to specify them.
`genotFitness` | A matrix or data frame that contains explicitly the mapping of genotypes to fitness. For now, we only allow epistasis-like relations between genes (so you cannot code order effects this way). Genotypes can be specified in two ways: As a matrix (or data frame) with g + 1 columns (where g > 1). Each of the first g columns contains a 1 or a 0 indicating that the gene of that column is mutated or not. Column g+ 1 contains the fitness values. This is, for instance, the output you will get from `rfitness`. If the matrix has all columns named, those will be used for the names of the genes. Of course, except for column or row names, all entries in this matrix or data frame must be numeric. As a two column data frame. The second column is fitness, and the first column are genotypes, given as a character vector. For instance, a row "A, B" would mean the genotype with both A and B mutated. In all cases, fitness must be `>= 0`. If any possible genotype is missing, its fitness is assumed to be 0, except for WT (if WT is missing, its fitness is assumed to be 1 —see examples).
`keepInput` | If TRUE, whether to keep the original input. This is only useful for human consumption of the output. It is useful because it is easier to decode, say, the restriction table from the data frame than from the internal representation. But if you want, you can set it to FALSE and the object will be a little bit smaller.

### Details

`allFitnessEffects` is used for extremely flexible specification of fitness and mutator effects, including posets, XOR relationships, synthetic mortality and synthetic viability, arbitrary forms of epistatis, arbitrary forms of order effects, etc. Please, see the vignette for detailed and commented examples.

`allMutatorEffects` provide the same flexibility, but without order and posets (this might be included in the future, but I have seen no empirical or theoretical argument for their existence or relevance as of now, so I do not add them to minimize unneeded complexity).

If you use both for simulations in the same call to, say, `oncoSimulIndiv`, all the genes specified in `allMutatorEffects` MUST be included in the `allFitnessEffects` object. If you want to have genes that have no direct effect on fitness, but that affect mutation rate, you MUST specify them in the call to `allFitnessEffects`, for instance as `noIntGenes` with an effect of 0.

If you use `genotFitness` then you cannot pass modules, noIntgenes, epistasis, or rT. This makes sense, because using `genotFitness` is saying "this is the mapping of genotypes to fitness. Period", so we should not allow further modifications from other terms.

If you use `genotFitness` you need to be careful when you use Bozic's model (as you get a death rate of 0).

If you use `genotFitness` note that we force the WT (wildtype) to always be 1 so fitnesses are rescaled.

### Value

An object of class "fitnessEffects" or "mutatorEffects". This is just a list, but it is not intended for human consumption. The components are:

`long.rt` | The restriction table in "long format", so as to be easy to parse by the C++ code.
`long.epistasis` | Ditto, but for the epistasis specification.
`long.orderEffects` | Ditto for the order effects.
`long.geneNoInt` | Ditto for the non-interaction genes.
`geneModule` | Similar, for the gene-module correspondence.
`graph` | An `igraph` object that shows the restrictions, epistasis and order effects, and is useful for plotting.
`drv` | The numeric identifiers of the drivers. The numbers correspond to the internal numeric coding of the genes.
`rT` | If `keepInput` is TRUE, the original restriction table.
`epistasis` | If `keepInput` is TRUE, the original epistasis vector.
`orderEffects` | If `keepInput` is TRUE, the original order effects vector.
`noIntGenes` | If `keepInput` is TRUE, the original noIntGenes.

### Note

Please, note that the meaning of the fitness effects in the McFarland model is not the same as in the original paper; the fitness coefficients are transformed to allow for a simpler fitness function as a product of terms. This differs with respect to v.1. See the vignette for details.

The names of the genes and modules can be fairly arbitrary. But if you try hard you can confuse the parser. For instance, using gene or module names that contain "," or ":", or ">" is likely to get you into trouble. Of course, you know you should not try to use those characters because you know those characters have special meanings to separate names or indicate epistasis or order relationships. Right now, using those characters as names is caught (and result in stopping) if passed as names for noIntGenes.

### Author(s)

Ramon Diaz-Uriarte

### References

Diaz-Uriarte, R. (2015). Identifying restrictions in the order of accumulation of mutations during tumor progression: effects of passengers, evolutionary models, and sampling http://www.biomedcentral.com/1471-2105/16/41/abstract

McFarland, C.~D. et al. (2013). Impact of deleterious passenger mutations on cancer progression. Proceedings of the National Academy of Sciences of the United States of America\/, 110(8), 2910–5.

### See Also

`evalGenotype`, `oncoSimulIndiv`, `plot.fitnessEffects`, `evalGenotypeFitAndMut`, `rfitness`, `plotFitnessLandscape`

### Examples

    ## A simple poset or CBN-like example

    cs <-  data.frame(parent = c(rep("Root", 4), "a", "b", "d", "e", "c"),
                     child = c("a", "b", "d", "e", "c", "c", rep("g", 3)),
                     s = 0.1,
                     sh = -0.9,
                     typeDep = "MN")

    cbn1 <- allFitnessEffects(cs)

    plot(cbn1)

    ## A more complex example, that includes a restriction table
    ## order effects, epistasis, genes without interactions, and moduels
    p4 <- data.frame(parent = c(rep("Root", 4), "A", "B", "D", "E", "C", "F"),
                     child = c("A", "B", "D", "E", "C", "C", "F", "F", "G", "G"),
                     s = c(0.01, 0.02, 0.03, 0.04, 0.1, 0.1, 0.2, 0.2, 0.3, 0.3),
                     sh = c(rep(0, 4), c(-.9, -.9), c(-.95, -.95), c(-.99, -.99)),
                     typeDep = c(rep("--", 4),
                         "XMPN", "XMPN", "MN", "MN", "SM", "SM"))

    oe <- c("C > F" = -0.1, "H > I" = 0.12)
    sm <- c("I:J"  = -1)
    sv <- c("-K:M" = -.5, "K:-M" = -.5)
    epist <- c(sm, sv)

    modules <- c("Root" = "Root", "A" = "a1",
                 "B" = "b1, b2", "C" = "c1",
                 "D" = "d1, d2", "E" = "e1",
                 "F" = "f1, f2", "G" = "g1",
                 "H" = "h1, h2", "I" = "i1",
                 "J" = "j1, j2", "K" = "k1, k2", "M" = "m1")

    set.seed(1) ## for repeatability
    noint <- rexp(5, 10)
    names(noint) <- paste0("n", 1:5)

    fea <- allFitnessEffects(rT = p4, epistasis = epist, orderEffects = oe,
                             noIntGenes = noint, geneToModule = modules)

    plot(fea)

    ## Modules that show, between them,
    ## no epistasis (so multiplicative effects).
    ## We specify the individual terms, but no value for the ":".

    fnme <- allFitnessEffects(epistasis = c("A" = 0.1,
                                            "B" = 0.2),
                              geneToModule = c("A" = "a1, a2",
                                               "B" = "b1"))

    evalAllGenotypes(fnme, order = FALSE, addwt = TRUE)

    ## Epistasis for fitness and simple mutator effects

    fe <- allFitnessEffects(epistasis = c("a : b" = 0.3,
                                              "b : c" = 0.5),
                                noIntGenes = c("e" = 0.1))

    fm <- allMutatorEffects(noIntGenes = c("a" = 10,
                                           "c" = 5))

    evalAllGenotypesFitAndMut(fe, fm, order = FALSE)

    ## Simple fitness effects (noIntGenes) and modules
    ## for mutators

    fe2 <- allFitnessEffects(noIntGenes =
                             c(a1 = 0.1, a2 = 0.2,
                               b1 = 0.01, b2 = 0.3, b3 = 0.2,
                               c1 = 0.3, c2 = -0.2))

    fm2 <- allMutatorEffects(epistasis = c("A" = 5,
                                           "B" = 10,
                                           "C" = 3),
                             geneToModule = c("A" = "a1, a2",
                                              "B" = "b1, b2, b3",
                                              "C" = "c1, c2"))

    evalAllGenotypesFitAndMut(fe2, fm2, order = FALSE)

    ## Passing fitness directly, a complete fitness specification
    ## with a two column data frame with genotypes as character vectors

    (m4 <- data.frame(G = c("A, B", "A", "WT", "B"), F = c(3, 2, 1, 4)))
    fem4 <- allFitnessEffects(genotFitness = m4)

    ## Verify it interprets what it should: m4 is the same as the evaluation
    ## of the fitness effects (note row reordering)
    evalAllGenotypes(fem4, addwt = TRUE, order = FALSE)

    ## Passing fitness directly, a complete fitness specification
    ## that uses a three column matrix

    m5 <- cbind(c(0, 1, 0, 1), c(0, 0, 1, 1), c(1, 2, 3, 5.5))
    fem5 <- allFitnessEffects(genotFitness = m5)

    ## Verify it interprets what it should: m5 is the same as the evaluation
    ## of the fitness effects
    evalAllGenotypes(fem5, addwt = TRUE, order = FALSE)

    ## Passing fitness directly, an incomplete fitness specification
    ## that uses a three column matrix

    m6 <- cbind(c(1, 1), c(1, 0), c(2, 3))
    fem6 <- allFitnessEffects(genotFitness = m6)
    evalAllGenotypes(fem6, addwt = TRUE, order = FALSE)

    ## Plotting a fitness landscape

    fe2 <- allFitnessEffects(noIntGenes =
                             c(a1 = 0.1,
                               b1 = 0.01,
                               c1 = 0.3))

    plot(evalAllGenotypes(fe2, order = FALSE))

    ## same as
    plotFitnessLandscape(evalAllGenotypes(fe2, order = FALSE))

    ## same as
    plotFitnessLandscape(fe2)

    ###### Defaults for missing genotypes

    ## As a two-column data frame

    (m8 <- data.frame(G = c("A, B, C", "B"), F = c(3, 2)))
    evalAllGenotypes(allFitnessEffects(genotFitness = m8), addwt = TRUE)

    ## As a matrix

    (m9 <- rbind(c(0, 1, 0, 1, 4), c(1, 0, 1, 0, 1.5)))
    evalAllGenotypes(allFitnessEffects(genotFitness = m9), addwt = TRUE)

    ## Reinitialize the seed
    set.seed(NULL)

[Package OncoSimulR version 2.18.0 Index]