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Related Concept Videos

Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
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Poisson Probability Distribution

A Poisson probability distribution is a discrete probability distribution. It gives the probability of a number of events occurring in a fixed interval of time or space if these events happen at a known average rate and independently of the time since the last event. For example, a book editor might be interested in the number of words spelled incorrectly in a particular book. It might be that, on average, there are five words spelled incorrectly in 100 pages. The interval is 100 pages.
The...
Mutation, Gene Flow, and Genetic Drift01:09

Mutation, Gene Flow, and Genetic Drift

In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).
Hardy-Weinberg Principle01:49

Hardy-Weinberg Principle

Diploid organisms have two alleles of each gene, one from each parent, in their somatic cells. Therefore, each individual contributes two alleles to the gene pool of the population. The gene pool of a population is the sum of every allele of all genes within that population and has some degree of variation. Genetic variation is typically expressed as a relative frequency, which is the percentage of the total population that has a given allele, genotype or phenotype.
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Exon Recombination

The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
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Following the Dynamics of Structural Variants in Experimentally Evolved Populations
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Published on: February 3, 2023

Evolutionary inference via the Poisson Indel Process.

Alexandre Bouchard-Côté1, Michael I Jordan

  • 1Department of Statistics, University of British Columbia, Vancouver, BC, Canada V6T 1Z4.

Proceedings of the National Academy of Sciences of the United States of America
|January 1, 2013
PubMed
Summary
This summary is machine-generated.

We introduce a new Poisson Indel Process (PIP) model for faster joint statistical inference of phylogenetic trees and sequence alignments. This model significantly improves computational efficiency compared to the traditional TKF91 model.

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Area of Science:

  • Computational Biology
  • Phylogenetics
  • Bioinformatics

Background:

  • Joint statistical inference of phylogenetic trees and multiple sequence alignments is crucial for understanding molecular evolution.
  • The classic Thorne, Kishino, and Felsenstein (TKF91) model, while foundational, presents computational intractability due to its exponential complexity in the number of taxa.
  • This intractability hinders efficient phylogenetic analysis of large datasets.

Purpose of the Study:

  • To develop a novel stochastic process for joint phylogenetic inference that overcomes the computational limitations of existing models.
  • To introduce a computationally efficient alternative to the TKF91 model for phylogenetic and sequence alignment analysis.
  • To enable scalable and accurate reconstruction of evolutionary histories.

Main Methods:

  • We propose the Poisson Indel Process (PIP), a stochastic process related to the TKF91 model but with a different treatment of insertions.
  • The PIP model is characterized as a Poisson process on the phylogeny, allowing for decoupled computations.
  • Bayesian inference methods are employed to compare the PIP model with separate inference approaches.

Main Results:

  • The PIP model reduces the computational complexity of joint phylogenetic inference from exponential to linear with respect to the number of taxa.
  • This linear complexity facilitates significantly faster and more scalable phylogenetic analyses.
  • Illustrative experiments demonstrate the effectiveness of Bayesian inference under the PIP model.

Conclusions:

  • The Poisson Indel Process (PIP) offers a computationally tractable and efficient framework for joint phylogenetic tree and multiple sequence alignment inference.
  • This advancement allows for more feasible analysis of large molecular sequence datasets.
  • The PIP model represents a significant improvement over the TKF91 model in terms of computational performance.