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Digital PCR-based Competitive Index for High-throughput Analysis of Fitness in Salmonella
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A general method for calculating likelihoods under the coalescent process.

K Lohse1, R J Harrison, N H Barton

  • 1Institute of Evolutionary Biology, University of Edinburgh, Edinburgh EH9 3JT, United Kingdom.

Genetics
|September 9, 2011
PubMed
Summary
This summary is machine-generated.

We developed a new method for analyzing genomic data, enabling efficient calculation of evolutionary relationships across many genetic loci. This approach is scalable for large genomic datasets with few mutations per sequence block.

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A Novel Bayesian Change-point Algorithm for Genome-wide Analysis of Diverse ChIPseq Data Types
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A Novel Bayesian Change-point Algorithm for Genome-wide Analysis of Diverse ChIPseq Data Types

Published on: December 10, 2012

Area of Science:

  • Population Genetics
  • Computational Biology
  • Genomic Data Analysis

Background:

  • Analyzing large genomic datasets requires efficient methods for calculating likelihoods across numerous loci.
  • Existing models often struggle with complex evolutionary processes like migration and recombination.

Purpose of the Study:

  • To present a general method for calculating the distribution of genealogies incorporating migration and recombination.
  • To demonstrate the scalability of likelihood calculations for genomic data analysis.

Main Methods:

  • Developed a method using linear recursions for the generating function of branch lengths.
  • Applied the infinite-sites model to determine mutation configuration probabilities.
  • Utilized Mathematica for automatic derivation of generating functions.

Main Results:

  • The method allows for explicit derivation of generating functions for complex models, such as the two-deme isolation-with-migration (IM) model.
  • Demonstrated feasibility by applying the method to simulated data and a large empirical dataset from Drosophila.
  • Showed that likelihood calculations are scalable to genomic data under specific conditions.

Conclusions:

  • The described method provides an efficient and scalable approach for analyzing large genomic datasets.
  • This technique facilitates maximum-likelihood estimation of population genetic model parameters.
  • The approach is particularly effective when dealing with a small number of sampled individuals and mutations per sequence block.