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The Fractional Coalescent
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A new approach to the coalescent, the
fractional
coalescent (
f
-coalescent), is introduced. Two derivations are presented: first, the
f
-coalescent is based on an extension of the discrete-time Wright-Fisher model. In this extension, for the population of size
N
, the probability that two randomly selected individuals have the same parent in the previous generation depends on the variable α. Second, the
f
-coalescent is based on an extension of the discrete-time Canning population model that the variance of the number of offspring is assumed as a random variable which depends on the variable α. In the second derivation, the
f
-coalescent emerges also as a continuous-time semi-Markov process. The additional parameter
α
affects the variability in the patterns of the waiting times; values of
α
< 1 lead to an increase of short time intervals, but allows occasionally for very long time intervals. When
α
= 1, the
f
-coalescent and Kingman’s
n
-coalescent are equivalent. The mode of the distribution of the time of the most recent common ancestor in the
f
-coalescent is lower than
n
-coalescent when the number of sample size increases, and the time which modes happen on that is smaller compare to
n
-coalescent. Also, this distribution showed that the
f
-coalescent leads to distributions with heavier tails than the
n
-coalescent. Also, the probability that
n
genes descend from
m
ancestral genes for
f
-coalescent is derived. The
f
-coalescent has been implemented in the population genetic model inference software M
IGRATE
. Simulation studies suggest that it is possible to infer the correct
α
values from data that was generated with known
α
values. When data is simulated using models with
α
< 1 or for three example datasets (H1N1 influenza, Malaria parasites, Humpback whales), Bayes factor comparisons show an improved model fit of the
f
-coalescent over the
n
-coalescent.
Title: The Fractional Coalescent
Description:
A new approach to the coalescent, the
fractional
coalescent (
f
-coalescent), is introduced.
Two derivations are presented: first, the
f
-coalescent is based on an extension of the discrete-time Wright-Fisher model.
In this extension, for the population of size
N
, the probability that two randomly selected individuals have the same parent in the previous generation depends on the variable α.
Second, the
f
-coalescent is based on an extension of the discrete-time Canning population model that the variance of the number of offspring is assumed as a random variable which depends on the variable α.
In the second derivation, the
f
-coalescent emerges also as a continuous-time semi-Markov process.
The additional parameter
α
affects the variability in the patterns of the waiting times; values of
α
< 1 lead to an increase of short time intervals, but allows occasionally for very long time intervals.
When
α
= 1, the
f
-coalescent and Kingman’s
n
-coalescent are equivalent.
The mode of the distribution of the time of the most recent common ancestor in the
f
-coalescent is lower than
n
-coalescent when the number of sample size increases, and the time which modes happen on that is smaller compare to
n
-coalescent.
Also, this distribution showed that the
f
-coalescent leads to distributions with heavier tails than the
n
-coalescent.
Also, the probability that
n
genes descend from
m
ancestral genes for
f
-coalescent is derived.
The
f
-coalescent has been implemented in the population genetic model inference software M
IGRATE
.
Simulation studies suggest that it is possible to infer the correct
α
values from data that was generated with known
α
values.
When data is simulated using models with
α
< 1 or for three example datasets (H1N1 influenza, Malaria parasites, Humpback whales), Bayes factor comparisons show an improved model fit of the
f
-coalescent over the
n
-coalescent.
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