Evidence map›Paper›PMID 32769100›Full record

ArticleGenetics2020

Estimation of Natural Selection and Allele Age from Time Series Allele Frequency Data Using a Novel Likelihood-Based Approach.

Zhangyi He, Xiaoyang Dai, Mark Beaumont, Feng Yu

Abstract read
In one paragraph

Article in Genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Zhangyi HeDepartment of Statistics, University of Oxford, OX1 3LB, United Kingdom z.he@imperial.ac.uk feng.yu@bristol.ac.uk.ORCID 0000-0002-5609-8962
Xiaoyang DaiSchool of Biological Sciences, University of Bristol, BS8 1TQ, United Kingdom.ORCID 0000-0002-3613-1219
Mark BeaumontSchool of Biological Sciences, University of Bristol, BS8 1TQ, United Kingdom.ORCID 0000-0002-8773-2743
Feng YuSchool of Mathematics, University of Bristol, BS8 1UG, United Kingdom z.he@imperial.ac.uk feng.yu@bristol.ac.uk.ORCID 0000-0003-0947-6809

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Temporally spaced genetic data allow for more accurate inference of population genetic parameters and hypothesis testing on the recent action of natural selection. In this work, we develop a novel likelihood-based method for jointly estimating selection coefficient and allele age from time series data of allele frequencies. Our approach is based on a hidden Markov model where the underlying process is a Wright-Fisher diffusion conditioned to survive until the time of the most recent sample. This formulation circumvents the assumption required in existing methods that the allele is created by mutation at a certain low frequency. We calculate the likelihood by numerically solving the resulting Kolmogorov backward equation backward in time while reweighting the solution with the emission probabilities of the observation at each sampling time point. This procedure reduces the two-dimensional numerical search for the maximum of the likelihood surface, for both the selection coefficient and the allele age, to a one-dimensional search over the selection coefficient only. We illustrate through extensive simulations that our method can produce accurate estimates of the selection coefficient and the allele age under both constant and nonconstant demographic histories. We apply our approach to reanalyze ancient DNA data associated with horse base coat colors. We find that ignoring demographic histories or grouping raw samples can significantly bias the inference results.

Indexed as

Gene FrequencyModels, GeneticSelection, GeneticAnimalsDiploidyDNA, AncientHumansLikelihood FunctionsMarkov ChainsDNA, Ancientallele ageconditioned Wright-Fisher diffusionhidden Markov modelmaximum likelihood estimationnatural selection

Identifiers

PMID32769100
PMCPMC7536852

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.