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Calculate the posterior marginal probabilities at a given variant using forward and backward tables propagated to that position.

Usage

PostProbs(
  fwd,
  bck,
  unif.on.underflow = FALSE,
  M = NULL,
  beta.theta.opts = NULL,
  nthreads = min(parallel::detectCores(logical = FALSE), fwd$to_recipient -
    fwd$from_recipient + 1)
)

Arguments

fwd

a forward table as returned by MakeForwardTable() and propagated to a target variant by Forward(). Must be at the same variant as bck (unless bck is in "beta-theta space" in which case if must be downstream ... see Backward() for details).

bck

a backward table as returned by MakeBackwardTable() and propagated to a target variant by Backward(). Must be at the same variant as fwd (unless bck is in "beta-theta space" in which case if must be downstream ... see Backward() for details).

unif.on.underflow

a logical; if TRUE, then if all probabilities in a column underflow, then they will be set to \(\frac{1}{N-1}\) instead of 0

M

a pre-existing matrix into which to write the probabilities, can yield substantial speed up but requires special attention (see Details)

beta.theta.opts

a list; see Details.

nthreads

the number of CPU cores to use. By default uses the parallel package to detect the number of physical cores.

Value

Matrix of posterior marginal probabilities. The \((j,i)\)-th element of of the returned matrix is the probability that \(j\) is copied by \(i\) at the current variant, \(l\), of the two tables, given the haplotypes observed (over the whole sequence).

Details

The forward and backward tables must be at the same variant in order for them to be combined to yield the posterior marginal probabilities at variant \(l\). The \((j,i)\)-th element of of the returned matrix is the probability that \(j\) is copied by \(i\) at the current variant, \(l\), of the two tables, given the haplotypes observed (over the whole sequence).

Note that each column represents an independent HMM.

By convention, every diagonal element is zero.

Notes on beta.theta.opts

In order to obtain posterior marginal probability matrices between variants fwd$l and bck$l, then bck must be in "beta-theta space", see Backward() for details. This allows the forward and backward tables to be transitioning both tables to some genomic position between fwd$l and bck$l. The precise recombination distance by which each table is propagated can be controlled by passing optional arguments in a list via beta.theta.opts. The recombination distances used can be specified in one of two ways.

  1. Manually. In this case, beta.theta.opts is a list containing two named elements:

    • "rho.fwd" \(\in (0,1)\) specifies the transition probability rho for propagating the forward table.

    • "rho.bck" \(\in (0,1)\) specifies the transition probability rho for propagating the backward table.

  2. Implicitly. In this case, beta.theta.opts is a list containing two named elements:

  • "pars": a kalisParameters object that implicitly defines the recombination distance \(\rho^\star\) between fwd$l and bck$l

  • "bias" \(\in (0,1)\). The forward table is propagated a distance of (bias)\(\rho^\star\) and the backward table is propagated a distance of (1-bias)\(\rho^\star\).

Performance notes

If calculating many posterior probability matrices in succession, providing a pre-existing matrix M that can be updated in-place can dramatically increase speed by eliminating the time needed for memory allocation. Be warned, since the matrix is updated in-place, if any other variables point to the same memory address, they will also be simultaneously overwritten. For example, writing

M <- matrix(0, nrow(fwd$alpha), ncol(fwd$alpha))
P <- M
PostProbs(fwd, bck, M = M)

will update M and P simultaneously.

When provided, M must have dimensions matching that of fwd$alpha. Typically, that is simply \(N \times N\) for \(N\) haplotypes. However, if kalis is being run in a distributed manner, M will be a \(N \times R\) matrix where \(R\) is the number of recipient haplotypes on the current machine.

See also

DistMat() to generate calculate \(d_{ji}\) distances directly; Forward() to propagate a Forward table to a new variant; Backward() to propagate a Backward table to a new variant

Examples

# To get the posterior probabilities at, say, variants 100 of the toy data
# built into kalis
data("SmallHaps")
data("SmallMap")

CacheHaplotypes(SmallHaps)
#> Warning: haplotypes already cached ... overwriting existing cache.

rho <- CalcRho(diff(SmallMap))
pars <- Parameters(rho)

fwd <- MakeForwardTable(pars)
bck <- MakeBackwardTable(pars)

Forward(fwd, pars, 100)
Backward(bck, pars, 100)

p <- PostProbs(fwd, bck)
d <- DistMat(fwd, bck)