Evidence map›Paper›PMID 37738175›Full record

ArticleMolecular biology and evolution2023

Inference of Coalescence Times and Variant Ages Using Convolutional Neural Networks.

Juba Nait Saada, Zoi Tsangalidou, Miriam Stricker, Pier Francesco Palamara

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Coalescence and translation: A language model for population genetics.Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Juba Nait SaadaDepartment of Statistics, University of Oxford, Oxford, UK.
Zoi TsangalidouDepartment of Statistics, University of Oxford, Oxford, UK.
Miriam StrickerDepartment of Statistics, University of Oxford, Oxford, UK.
Pier Francesco PalamaraDepartment of Statistics, University of Oxford, Oxford, UK.ORCID 0000-0002-7999-1972

Funding

Department of HealthMedical Research Council EP/L016044/1Medical Research Council MR/S502509/1Wellcome TrustWellcome Trust 203141/Z/16/ZWellcome Trust 204826/Z/16/Z
6 · The paper itself

Abstract

Accurate inference of the time to the most recent common ancestor (TMRCA) between pairs of individuals and of the age of genomic variants is key in several population genetic analyses. We developed a likelihood-free approach, called CoalNN, which uses a convolutional neural network to predict pairwise TMRCAs and allele ages from sequencing or SNP array data. CoalNN is trained through simulation and can be adapted to varying parameters, such as demographic history, using transfer learning. Across several simulated scenarios, CoalNN matched or outperformed the accuracy of model-based approaches for pairwise TMRCA and allele age prediction. We applied CoalNN to settings for which model-based approaches are under-developed and performed analyses to gain insights into the set of features it uses to perform TMRCA prediction. We next used CoalNN to analyze 2,504 samples from 26 populations in the 1,000 Genome Project data set, inferring the age of ∼80 million variants. We observed substantial variation across populations and for variants predicted to be pathogenic, reflecting heterogeneous demographic histories and the action of negative selection. We used CoalNN's predicted allele ages to construct genome-wide annotations capturing the signature of past negative selection. We performed LD-score regression analysis of heritability using summary association statistics from 63 independent complex traits and diseases (average N=314k), observing increased annotation-specific effects on heritability compared to a previous allele age annotation. These results highlight the effectiveness of using likelihood-free, simulation-trained models to infer properties of gene genealogies in large genomic data sets.

Indexed as

GenomeNeural Networks, ComputerComputer SimulationGenomicsHumansModels, GeneticMultifactorial InheritancePolymorphism, Single Nucleotideallele agecoalescence timeheritabilitymachine learningnatural selection

Identifiers

PMID37738175
PMCPMC10581698

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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.