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Estimate of within population incremental selection through branch imbalance in lineage trees
Author(s) -
Gilad Liberman,
Jennifer I. C. Benichou,
Yaakov Maman,
Jacob Glanville,
Idan Alter,
Yoram Louzoun
Publication year - 2015
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkv1198
Subject(s) - biology , selection (genetic algorithm) , lineage (genetic) , mutation rate , population , mutation , neutral mutation , effective population size , genetics , negative selection , tree (set theory) , evolutionary biology , gene , genetic variation , genome , mathematics , machine learning , computer science , mathematical analysis , demography , sociology
Incremental selection within a population, defined as limited fitness changes following mutation, is an important aspect of many evolutionary processes. Strongly advantageous or deleterious mutations are detected using the synonymous to non-synonymous mutations ratio. However, there are currently no precise methods to estimate incremental selection. We here provide for the first time such a detailed method and show its precision in multiple cases of micro-evolution. The proposed method is a novel mixed lineage tree/sequence based method to detect within population selection as defined by the effect of mutations on the average number of offspring. Specifically, we propose to measure the log of the ratio between the number of leaves in lineage trees branches following synonymous and non-synonymous mutations. The method requires a high enough number of sequences, and a large enough number of independent mutations. It assumes that all mutations are independent events. It does not require of a baseline model and is practically not affected by sampling biases. We show the method's wide applicability by testing it on multiple cases of micro-evolution. We show that it can detect genes and inter-genic regions using the selection rate and detect selection pressures in viral proteins and in the immune response to pathogens.

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