The hardware and bandwidth for this mirror is donated by dogado GmbH, the Webhosting and Full Service-Cloud Provider. Check out our Wordpress Tutorial.
If you wish to report a bug, or if you are interested in having us mirror your free-software or open-source project, please feel free to contact us at mirror[@]dogado.de.
library(MethEvolSIM)MethEvolSIM is an R package for simulating DNA methylation dynamics on different genomic structures along a given tree. It allows simulating methylation and demethylation events at loci within two different types of genomic structures: regions with low methylation or with high methylation. The data can be interpreted as:
1- CpG sites inside or outside CpG islands or
2- any type of methylation site in regions of higher or lower methylation or
3- CpG islands inside or outside genomic archipelagos (regions with many CpG islands).
In this document, unless specified otherwise, we use the first interpretation.
As a simple example with default parameter values we show a simulation of evolution of a simplified genomic structure on a tree:
# Define the tree:
tree <- "((a:1, b:1):2, c:2);"
# Define the genomic structure. Here 1 island ("U") containing 100 CpGs
# surrounded by 2 non-island structures ("M") each containing 10 CpGs
infoStr <- data.frame(n = c(10, 100, 10),
globalState = c("M", "U", "M"))
# Simulate 1 replicate of data at the tree tips
output <- simulate_evolData(infoStr = infoStr, tree = tree)
#> Using default parameter values
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2);In the simulation output 0 stands for unmethylated, 1 for methylated and 0.5 for partially methylated or hemimethylated.
# In replicate 1, tip 2: name of the tip of the tree
output$data[[1]][[2]]$name
#> [1] "b"
# In replicate 1, tip 2: sequence of methylation states of left non-island structure
output$data[[1]][[2]]$seq[[1]]
#> [1] 1 1 1 1 1 1 1 1 1 1
# In replicate 1, tip 2: sequence of methylation states of island structure
output$data[[1]][[2]]$seq[[2]]
#> [1] 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
#> [38] 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
#> [75] 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0
# In replicate 1, tip 2: sequence of methylation states of right non-island structure
output$data[[1]][[2]]$seq[[3]]
#> [1] 0 0 1 1 1 1 1 1 1 1Structures are categorized as CpG islands or non-islands (alternatively regions with low/high methylation or archipelagos/non-archipelagos). In the root of the genealogy we assume that each structure samples an equilibrium probability triple \((\pi_u,\pi_p, \pi_m)\) for the methylation states: unmethylated, partially-methylated and methylated, respectively. Current parameter values favor prevalent homogeneity in methylation levels within structures, most CpG islands predominantly unmethylated and a small proportion predominantly methylated, and most non-islands predominantly methylated and a small proportion predominantly unmethylated. The sampling of the equilibrium probability triple is done using two distinct Beta distributions to sample the corresponding methylation frequencies.
Island parameterization: alpha_pI, beta_pI, alpha_mI, beta_mI
MethEvolSIM samples \(\pi_p\) from the first Beta distribution. Current parameterization uses as initial parameter values a relatively small \(\alpha_{I_p}\) and relatively large \(\beta_{I_p}\) to encourage minor assignment of partially methylated states.
The second Beta distribution, scaled by \(1 - \pi_p\), corresponds to the proportion of methylated and unmethylated states. Currently both parameter values (\(\alpha_{I_m}\) and \(\beta_{I_m}\)) set to small values while \({\alpha_{I_m} < \beta_{I_m}}\) to favour shifting the stochastic choice toward homogeneous states with a higher proportion of predominantly unmethylated islands, and assigned to \(\pi_m\). Finally, we set \(\pi_u\) as \(1 - \pi_p - \pi_m\).
Non-island parameterization: alpha_pNI, beta_pNI, alpha_mNI, beta_mNI
Following the same rationale as for island parameterization, each non-island structure samples a common equilibrium probability triple from two Beta distributions with parameters \(\alpha_{NI_p}\), \(\beta_{NI_p}\), \(\alpha_{NI_m}\) and \(\beta_{NI_m}\). The parameter values are currently set to favor the characteristic high overall methylation level.
Parameter ranges The alpha and beta parameters of a Beta distribution must be greater than 0, that is in (0, \(\infty\)).
DNA methylation state evolution happens by two structure-specific events: CpG single site events (SSEs) and CpG island wide events (IWEs).
IWEs change the island methylation probabilities and some of the CpG sites in the CpG island can simultaneously change their state at the same time. Different CpG islands, however, are assumed to evolve independently of each other. IWEs occur per CpG island at a rate denoted by \(\mu\). Consequently, over a branch of length \(l\), the expected number of IWEs per island is given by \(\mu \cdot l\).
IWE parameterization: mu. Parameter range: Should be a small number, but it can take any value from 0, that is in \([0, \infty)\)
In addition to IWEs we allow for single site events (SSEs), which change the methylation states of single CpG sites within and between CpG islands. In our model SSEs account for two dynamics: independent of each other (SSEi), and assuming correlations between adjacent sites (SSEc).
As SSEc transition probabilities are dependent on adjacent sites we use Gillespie’s \(\tau\)-leap approximation. to allow for CpG sites to o update their neighbouring state and rates of change after short time steps. Therefore, we first discretize the branch intervals between IWEs in time intervals of default length \(dt =0.01\). For each CpG position and each time interval the rate matrix for the transitions between the states unmethylated, partially methylated and methylated results from the addition of the rate matrices of the two types of SSE events, so that \(\mathbb{E}(R_i + R_c)=1\), \(R_i\) and \(R_c\) representing the rate factors of independent and correlated processes. The independent process samples the new methylation state from the structure’s equilibrium frequencies and the correlated process copies the left or right neighbor state with equal probabilities. The proportion of each of the two SSE types is determined by the model parameter \(\iota\).
Different positions \(j\) have different SSEi rates \(R_{i,j}\) coming from a discretized gamma distribution with 3 categories, expected value \(\iota\) and shape parameters \(\alpha_{R_{i}}\) and \({\beta_{R_{i}}}=\frac{\alpha_{R_{i}}}{\iota}\). The probability to be in each respective rate category is 1/3. For the rate of collaborative SSEs \(R_c = 1-\iota\), the probability of considering left of right neighbour is equal.
SSE process parameterization: iota, alpha_Ri Parameter ranges The alpha parameter of a Gamma distribution must be greater than 0, that is (0, \(\infty\)). Iota must be between 0 (non-included) and 1, that is in (0,1]. Note that due to numerical limitations, the smallest value of both parameters used by MethEvolSIM is 0.01.
The initial spatial distribution of CpG sites in islands and non-island structures is given by the user through a data frame with 2 columns named “n” and “globalState” , which encode the structural information. Each row provides the information of a different genomic structure.
n number of positions for each structure (e.g. number of CpG sites).
globalState encodes island and non-island structures with the character value “U” for unmethylated regions (e.g. CpG islands) and “M” for methylated regions (e.g. non-CpG islands).
# Example 3 structures of length 100 each:
# one non-island containing 100 CpG sites,
# one island containing 100 CpG sites,
# and one non-island containing 100 CpG sites
infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"))
infoStr
#> n globalState
#> 1 100 M
#> 2 100 U
#> 3 100 M# Example for 2 islands: first of length 1, second of length 15
infoStr <- data.frame(n = c(1, 15),
globalState = c("U", "U"))
infoStr
#> n globalState
#> 1 1 U
#> 2 15 UThe initial methylation state distribution assigns a triple of methylation equilibrium frequencies() \(\pi_u\) for unmethylated, \(\pi_p\) for partially-methylated, and \(\pi_m\) for methylated) to each of the simulated genomic structures. This assignation can be done in two ways:
1 - Sampled as specified in the section “Model parameters: Initial
methylation state distribution” when the given infoStr only
contains n and globalState columns.
2 - Determined by the user providing in infoStr
additional columns: u_eqFreq for \(\pi_u\), p_eqFreq for \(\pi_p\) and m_eqFreq for \(\pi_m\). Note that when given, the triple
of frequency values for each of the structures needs to sum up to 1, so
that for each row \(i\), \(\pi_u(i)+\pi_p(i)+\pi_m(i)=1\).
# Example 3 structures of length 100 with customized initial methylation state
# equilibrium frequencies
infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"),
u_eqFreq = c(0.1, 0.8, 0.1),
p_eqFreq = c(0.1, 0.1, 0.1),
m_eqFreq = c(0.8, 0.1, 0.8))
infoStr
#> n globalState u_eqFreq p_eqFreq m_eqFreq
#> 1 100 M 0.1 0.1 0.8
#> 2 100 U 0.8 0.1 0.1
#> 3 100 M 0.1 0.1 0.8The default parameter values used by MethEvolSIM can be obtained
using the function get_parameterValues(), which returns a
data frame with the columns named as specified in the section “Model
parameters”:
default_paramValues <- get_parameterValues()
default_paramValues
#> alpha_pI beta_pI alpha_mI beta_mI alpha_pNI beta_pNI alpha_mNI beta_mNI mu
#> 1 0.1 1 0.1 0.5 0.1 1 0.5 0.1 0.1
#> alpha_Ri iota Ri1 Ri2 Ri3
#> 1 0.1 0.3 2.80506e-06 0.005770752 0.8942264Additionally, it returns the three rates of change for SSEi
process,Ri1, Ri2, and Ri3 (see
section “Model Parameters: Single-site events (SSEs)”).
The section “Model parameters” provides further information about
each of the parameters, including the range of possible values for each
parameter. To simulate data with a different parameterization, the new
value of the chosen parameter(s) can be modified in the data frame, but
for the cases of Ri1, Ri2, and
Ri3, which are modified through iota and
alpha_Ri.
# Example: modification of parameter iota to value 0.2
default_paramValues$iota <- 0.2
default_paramValues
#> alpha_pI beta_pI alpha_mI beta_mI alpha_pNI beta_pNI alpha_mNI beta_mNI mu
#> 1 0.1 1 0.1 0.5 0.1 1 0.5 0.1 0.1
#> alpha_Ri iota Ri1 Ri2 Ri3
#> 1 0.1 0.2 2.80506e-06 0.005770752 0.8942264Additional details regarding the get_parameterValues()
function can be found in its documentation.
DNA Methylation Data is simulated using three R6 classes:
singleStructureGenerator,
combiStructureGenerator, and
treeMultiRegionSimulator. Instances of the
singleStructureGenerator class represent individual genomic
structures (e.g. islands or non-islands) and are encapsulated within
instances of the combiStructureGenerator class, which, in
turn, represent the simulated data structure (e.g. a sequence consisting
of a non-island containing 100 CpGs, an island containing 100 CpGs, and
a non-island containing 100 CpGs). Finally, instances of the
treeMultiRegionSimulator class contain a
combiStructureGenerator object at each node of a given
tree, including its root and leaves.
Generally, simulations are conducted as explained in subsection
“Simulation of Data Evolution”, with a documented user-interface
function explaining the output structure:
simulate_evolData(). Alternativelly, the user can simulate
initial data so that the root of the tree is fixed as explained in
subsection “Simulation of Initial Data”. The latter option generates
objects of class combiStructureGenerator containing objects
of class singleStructureGenerator. In the subsection
“Simulation of Initial Data: Exploration of Initial Data” an example to
interact with the classes is given, while further information about the
attributes and methods of each class is provided in their
documentation.
The initial data can be generated as an object of class
combiStructureGenerator.
# Example with customized initial methylation frequencies and customized parameter values
custom_infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"),
u_eqFreq = c(0.1, 0.8, 0.1),
p_eqFreq = c(0.1, 0.1, 0.1),
m_eqFreq = c(0.8, 0.1, 0.8))
custom_params <- get_parameterValues()
custom_params$mu <- 0.005
initial_customD <- simulate_initialData(infoStr = custom_infoStr, params = custom_params)
# Returns customized parameters and simulated data
initial_customD$params
#> alpha_pI beta_pI alpha_mI beta_mI alpha_pNI beta_pNI alpha_mNI beta_mNI mu
#> 1 0.1 1 0.1 0.5 0.1 1 0.5 0.1 0.005
#> alpha_Ri iota Ri1 Ri2 Ri3
#> 1 0.1 0.3 2.80506e-06 0.005770752 0.8942264
initial_customD$data
#> <combiStructureGenerator>
#> Public:
#> add_offspring_index: function (i)
#> branch_evol: function (branch_length, dt, testing = FALSE)
#> clone: function (deep = FALSE)
#> copy: function ()
#> get_island_index: function ()
#> get_island_number: function ()
#> get_IWE_events: function ()
#> get_mu: function ()
#> get_name: function ()
#> get_offspring_index: function ()
#> get_own_index: function ()
#> get_parent_index: function ()
#> get_singleStr: function (i)
#> get_singleStr_number: function ()
#> initialize: function (infoStr, params = NULL, testing = FALSE)
#> set_IWE_events: function (a)
#> set_name: function (a)
#> set_offspring_index: function (i)
#> set_own_index: function (i)
#> set_parent_index: function (i)
#> set_singleStr: function (singStrList)
#> Private:
#> interval_evol: function (interval_length, dt, testing = FALSE)
#> IWE_events: NULL
#> IWE_rate: 0.005
#> mu: 0.005
#> name: NULL
#> offspring_index: NULL
#> own_index: NULL
#> parent_index: NULL
#> set_IWE_rate: function ()
#> singleStr: list
#> singleStr_globalState: M U M
#> SSE_evol: function (dt, testing = FALSE)# Example with sampled initial methylation frequencies and default parameter values
custom_infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"))
initialD <- simulate_initialData(infoStr = custom_infoStr)
# Returns default parameters
initialD$params
#> alpha_pI beta_pI alpha_mI beta_mI alpha_pNI beta_pNI alpha_mNI beta_mNI mu
#> 1 0.1 1 0.1 0.5 0.1 1 0.5 0.1 0.1
#> alpha_Ri iota Ri1 Ri2 Ri3
#> 1 0.1 0.3 2.80506e-06 0.005770752 0.8942264
initialD$data
#> <combiStructureGenerator>
#> Public:
#> add_offspring_index: function (i)
#> branch_evol: function (branch_length, dt, testing = FALSE)
#> clone: function (deep = FALSE)
#> copy: function ()
#> get_island_index: function ()
#> get_island_number: function ()
#> get_IWE_events: function ()
#> get_mu: function ()
#> get_name: function ()
#> get_offspring_index: function ()
#> get_own_index: function ()
#> get_parent_index: function ()
#> get_singleStr: function (i)
#> get_singleStr_number: function ()
#> initialize: function (infoStr, params = NULL, testing = FALSE)
#> set_IWE_events: function (a)
#> set_name: function (a)
#> set_offspring_index: function (i)
#> set_own_index: function (i)
#> set_parent_index: function (i)
#> set_singleStr: function (singStrList)
#> Private:
#> interval_evol: function (interval_length, dt, testing = FALSE)
#> IWE_events: NULL
#> IWE_rate: 0.1
#> mu: 0.1
#> name: NULL
#> offspring_index: NULL
#> own_index: NULL
#> parent_index: NULL
#> set_IWE_rate: function ()
#> singleStr: list
#> singleStr_globalState: M U M
#> SSE_evol: function (dt, testing = FALSE)To get the parameter values of a combiStructureGenerator
object, it can alternativelly be given as argument to the function
get_parameterValues().
combiStr_object <- initialD$data
get_parameterValues(rootData = combiStr_object)
#> alpha_pI beta_pI alpha_mI beta_mI alpha_pNI beta_pNI alpha_mNI beta_mNI mu
#> 1 0.1 1 0.1 0.5 0.1 1 0.5 0.1 0.1
#> alpha_Ri iota Ri1 Ri2 Ri3
#> 1 0.1 0.3 2.80506e-06 0.005770752 0.8942264The methods of the class combiStructureGenerator can be
used to access each of the contained structures:
# E.g. access fist structure (non-island)
combiStr_object$get_singleStr(1)Each contained structure is an object of
singleStructureGenerator and its methods can be used to get
the contained information.
# E.g. get the methylation equilibrium frequencies of the first singleStructureGenerator
combiStr_object$get_singleStr(1)$get_eqFreqs()
#> [1] 0.77331702 0.19727515 0.02940782# E.g. get the sequence of methylation states of the second singleStructureGenerator
# Encoded as: 1 for unmethylated, 2 for partially-methylated, 3 for methylated
combiStr_object$get_singleStr(2)$get_seq()
#> [1] 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1
#> [38] 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1
#> [75] 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1The evolution data is generated with the function
simulate_evolData(). It returns the parameters used
($params), the length of the time step used for the
Gillespie’s \(\tau\)-leap approximation
($dt, default 0.01), the tree used ($tree),
and the simulated data ($data). The description of the
simulated data is available in the function’s documentation.
It takes as parameters:
tree: A string representing a tree in Newick
format.
infoStr: A dataframe with the information of the
number of CpGs corresponding to each island and non-island region
(columns named n and globalState).
Additionally the initial methylation frequencies can be specified adding
the columns u_eqFreq, p_eqFreq and
m_eqFreq.
dt: The length of time steps for Gillespie’s \(\tau\)-leap approximation. Numerical,
default is 0.01.
n_rep: The number of replicates. Integer, default is
1.
only_tip: Logical indicating whether to extract data
only for tips (TRUE, default) or to extract the information for all the
tree branches (FALSE).
params: Default NULL for simulation with default
parameter values. When customized parameter values are used the output
dataframe of get_parameterValues() can be modified and
given to the function. E.g:
# Example with customized initial methylation frequencies, customized parameter values
# and default dt (0.01)
tree <- "((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);"
custom_infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"),
u_eqFreq = c(0.1, 0.8, 0.1),
p_eqFreq = c(0.1, 0.1, 0.1),
m_eqFreq = c(0.8, 0.1, 0.8))
custom_params <- get_parameterValues()
custom_params$mu <- 0.005
evolD <- simulate_evolData(infoStr = custom_infoStr, tree = tree, params = custom_params, n_rep = 3, only_tip = TRUE)
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);# Returns customized parameters, tree used, time step length for SSE process used (dt)
# and simulated data
evolD$data
evolD$dt
evolD$tree
evolD$params# The simulated data is returned as a list. Each element of the list corresponds to a
# simulation replicate:
length(evolD$data)
#> [1] 3
rep1 <- evolD$data[[1]]
rep2 <- evolD$data[[2]]
rep3 <- evolD$data[[3]]# When only_tip is TRUE, each replicate contains for each tip: its name and the
# sequence of methylation states. E.g.
rep1_tip1 <- rep1[[1]]
rep1_tip1$name
#> [1] "a"
# Seq is a list with the methylation states of each simulated structure.
# In this example, 3 structures: non-island, island and non-island ...
length(rep1_tip1$seq)
#> [1] 3
# Each with 100 CpGs
length(rep1_tip1$seq[[1]])
#> [1] 100When simulations are conducted with only_tip = FALSE the
$data output contains more information.
tree <- "((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);"
custom_infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"),
u_eqFreq = c(0.1, 0.8, 0.1),
p_eqFreq = c(0.1, 0.1, 0.1),
m_eqFreq = c(0.8, 0.1, 0.8))
custom_params <- get_parameterValues()
custom_params$mu <- 0.005
evolD <- simulate_evolData(infoStr = custom_infoStr, tree = tree, params = custom_params, n_rep = 3, only_tip = FALSE)
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);
#> Simulating data at root and letting it evolve along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);# When only_tip is FALSE. $data output contains the simulated data and the
# information on the relationship between tree branches.
names(evolD$data)
#> [1] "sim_data" "branchInTree"# The information of the tree branches can be accessed using $branchInTree.
treeStr <- evolD$data$branchInTree
# It is a list in which each element index represents the index of the branch
root <- treeStr[[1]] # First branch (or tree root)
b2 <- treeStr[[2]] # Second branch
# ...
# Each branch contains information of the offspring and parent indexes.
root$parent_index # The tree root does not have parent branches
#> NULL
root$offspring_index # The tree root has 3 daughter branches: 2, 5 and 6.
#> [1] 2 5 6
b2$parent_index # Branch 2 therefore has as parent branch the root.
#> [1] 1
b2$offspring_index # Branch 2 also has 2 daughter branches: 3 and 4
#> [1] 3 4# The simulated data can be accessed using $sim_data.
sim_data <- evolD$data$sim_data
# As before, each list element corresponds to a simulation replicate.
# E.g. replicate 3
rep3 <- sim_data[[3]]
# In each replicate, each element of the list corresponds to a tree branch
# the indexes correspond to the information in $branchInTree
root <- rep3[[1]]
b2 <- rep3[[2]]
b3 <- rep3[[3]]# Each tree branch contains:
# - the branch name (NULL for tree root and inner nodes and
# tip name for the tree tips):
root$name
#> NULL
b2$name
#> NULL
b3$name
#> [1] "a"# - the information on IWE events that happened in that branch.
root$IWE # The root always has NULL because its branch length is 0
#> NULL
# The rest of the branches have FALSE when no IWE happened or a list containing
# $islands corresponds to the island index(es) to which the event(s) happened
# $times corresponds to the branch time in which the event happened.
b2$IWE
#> [1] FALSE
b3$IWE
#> [1] FALSE# - A list with each element representing the sequence of methylation states of
# each simulated island and non-island
# Encoded as 0 for unmethylated, 0.5 for partially methylated and 1 for methylated
root$seq[[1]] # First sequence (non-island)
#> [1] 1.0 0.5 1.0 1.0 0.0 1.0 1.0 1.0 1.0 1.0 1.0 1.0 0.0 0.5 0.0 1.0 1.0 1.0
#> [19] 0.0 1.0 1.0 1.0 1.0 1.0 1.0 0.0 0.5 1.0 1.0 1.0 0.5 1.0 1.0 1.0 1.0 1.0
#> [37] 1.0 0.0 0.5 1.0 1.0 1.0 1.0 1.0 1.0 1.0 1.0 1.0 1.0 0.5 1.0 1.0 1.0 1.0
#> [55] 1.0 0.5 1.0 0.0 0.0 1.0 1.0 0.0 0.0 1.0 1.0 0.5 1.0 0.0 1.0 1.0 1.0 1.0
#> [73] 1.0 1.0 1.0 0.5 1.0 1.0 1.0 0.0 1.0 1.0 1.0 1.0 0.5 1.0 1.0 1.0 1.0 1.0
#> [91] 1.0 1.0 1.0 1.0 1.0 0.0 1.0 1.0 1.0 1.0
root$seq[[2]] # Second sequence (island)
#> [1] 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 1.0 0.5 0.0 0.0 0.0
#> [19] 0.0 0.0 0.0 0.5 0.0 1.0 1.0 0.0 0.0 1.0 0.0 0.0 0.0 0.0 1.0 0.0 0.0 0.0
#> [37] 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 1.0 0.0 1.0 0.0 0.0 0.5 0.0 0.5
#> [55] 0.0 0.0 0.0 0.0 0.0 0.0 0.0 1.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.5
#> [73] 0.5 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 1.0 0.0 0.0 1.0 1.0 0.0 0.0
#> [91] 0.0 1.0 0.0 0.0 0.0 0.0 0.0 0.0 1.0 1.0# - A list with each element representing the methylation frequencies for the states: unmethylated, partially-methylated and methylated
root$eqFreqs[[1]][1] # First structure of root (non-island) equilibrium frequency for unmethylated state
#> [1] 0.1
root$eqFreqs[[1]][2] # First structure of root (non-island) equilibrium frequency for partially-methylated state
#> [1] 0.1
root$eqFreqs[[1]][3] # First structure of root (non-island) equilibrium frequency for methylated state
#> [1] 0.8rootData: Alternative argument to infoStr
(only one can be given). It enables simulating replicates of evolution
along a tree with fixed data at root. When used, it takes the output of
simulate_initialData()$data. If customized parameter values
are to be used, then the customized parameters are given to
simulate_initialData() instead to
simulate_evolData().# Example with customized initial methylation frequencies, customized parameter values and default dt (0.01)
tree <- "((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);"
custom_infoStr <- data.frame(n = c(100, 100, 100),
globalState = c("M", "U", "M"),
u_eqFreq = c(0.1, 0.8, 0.1),
p_eqFreq = c(0.1, 0.1, 0.1),
m_eqFreq = c(0.8, 0.1, 0.8))
custom_params <- get_parameterValues()
custom_params$mu <- 0.005
initialD <- simulate_initialData(infoStr = custom_infoStr, params = custom_params)$data
evolD <- simulate_evolData(rootData =initialD, tree = tree)
#> Parameter values set as in given rootData
#> Simulating evolution of given data at root along given tree: ((a:1, b:1):2, c:2, (d:3.7, (e:4, f:1):3):5);These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.