Egor Alimpiev | Searcharxiv

arXiv2021

A compendium of covariances and correlation coefficients of coalescent tree properties

Gene genealogies are frequently studied by measuring properties such as their height ($H$), length ($L$), sum of external branches ($E$), sum of internal branches ($I$), and mean of their two basal branches ($B$), and the coalescence times that contribute to the other genealogical features ($T$). These tree properties and their relationships can provide insight into the effects of population-genetic processes on genealogies and genetic sequences. Here, under the coalescent model, we study the 15 correlations among pairs of features of genealogical trees: $H_n$, $L_n$, $E_n$, $I_n$, $B_n$, and $T_k$ for a sample of size $n$, with $2 \leq k \leq n$. We report high correlations among $H_n$, $L_n$, $I_n,$ and $B_n$, with all pairwise correlations of these quantities having values greater than or equal to $\sqrt{6} [6 ζ(3) + 6 - π^2] / ( π\sqrt{18 + 9π^2 - π^4}) \approx 0.84930$ in the limit as $n \rightarrow \infty$. Although $E_n$ has an expectation of 2 for all $n$ and $H_n$ has expectation 2 in the limit as $n \rightarrow \infty$, their limiting correlation is 0. The results contribute toward understanding features of the shapes of coalescent trees.

q-bio.PE↗

arXiv2021

Enumeration of coalescent histories for caterpillar species trees and $p$-pseudocaterpillar gene trees

For a fixed set $X$ containing $n$ taxon labels, an ordered pair consisting of a gene tree topology $G$ and a species tree $S$ bijectively labeled with the labels of $X$ possesses a set of coalescent histories -- mappings from the set of internal nodes of $G$ to the set of edges of $S$ describing possible lists of edges in $S$ on which the coalescences in $G$ take place. Enumerations of coalescent histories for gene trees and species trees have produced suggestive results regarding the pairs $(G,S)$ that, for a fixed $n$, have the largest number of coalescent histories. We define a class of 2-cherry binary tree topologies that we term $p$-pseudocaterpillars, examining coalescent histories for non-matching pairs $(G,S)$, in the case in which $S$ has a caterpillar shape and $G$ has a $p$-pseudocaterpillar shape. Using a construction that associates coalescent histories for $(G,S)$ with a class of "roadblocked" monotonic paths, we identify the $p$-pseudocaterpillar labeled gene tree topology that, for a fixed caterpillar labeled species tree topology, gives rise to the largest number of coalescent histories. The shape that maximizes the number of coalescent histories places the "second" cherry of the $p$-pseudocaterpillar equidistantly from the root of the "first" cherry and from the tree root. A symmetry in the numbers of coalescent histories for $p$-pseudocaterpillar gene trees and caterpillar species trees is seen to exist around the maximizing value of the parameter $p$. The results provide insight into the factors that influence the number of coalescent histories possible for a given gene tree and species tree.

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