Evidence map›Paper›PMID 39152666›Full record

ArticleMolecular ecology resources2024

Estimation of spatial demographic maps from polymorphism data using a neural network.

Chris C R Smith, Gilia Patterson, Peter L Ralph, Andrew D Kern

Abstract read
In one paragraph

Article in Molecular ecology resources, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Chris C R SmithInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, USA.ORCID https://orcid.org/0000-0002-6470-3413
Gilia PattersonInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, USA.
Peter L RalphInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, USA.ORCID https://orcid.org/0000-0002-9459-6866
Andrew D KernInstitute of Ecology and Evolution, University of Oregon, Eugene, Oregon, USA.

Funding

Deep learning for population geneticsR01HG010774 · NHGRI · UNIVERSITY OF OREGON · PI ANDREW D KERN · 2020 to 2026
$3.2M
Computational Population GeneticsR35GM148253 · NIGMS · UNIVERSITY OF OREGON · PI ANDREW D KERN · 2023 to 2026
$1.5M
Deep learning for spatial population geneticsF32GM146484 · NIGMS · UNIVERSITY OF OREGON · PI SMITH, CHRIS C · 2022 to 2023
$122k
NHGRI NIH HHS R01 HG010774NIGMS NIH HHS F32 GM146484NIGMS NIH HHS R35 GM148253NIH HHS F32GM146484NIH HHS R01HG010774NIH HHS R35GM148253
6 · The paper itself

Abstract

A fundamental goal in population genetics is to understand how variation is arrayed over natural landscapes. From first principles we know that common features such as heterogeneous population densities and barriers to dispersal should shape genetic variation over space, however there are few tools currently available that can deal with these ubiquitous complexities. Geographically referenced single nucleotide polymorphism (SNP) data are increasingly accessible, presenting an opportunity to study genetic variation across geographic space in myriad species. We present a new inference method that uses geo-referenced SNPs and a deep neural network to estimate spatially heterogeneous maps of population density and dispersal rate. Our neural network trains on simulated input and output pairings, where the input consists of genotypes and sampling locations generated from a continuous space population genetic simulator, and the output is a map of the true demographic parameters. We benchmark our tool against existing methods and discuss qualitative differences between the different approaches; in particular, our program is unique because it infers the magnitude of both dispersal and density as well as their variation over the landscape, and it does so using SNP data. Similar methods are constrained to estimating relative migration rates, or require identity-by-descent blocks as input. We applied our tool to empirical data from North American grey wolves, for which it estimated mostly reasonable demographic parameters, but was affected by incomplete spatial sampling. Genetic based methods like ours complement other, direct methods for estimating past and present demography, and we believe will serve as valuable tools for applications in conservation, ecology and evolutionary biology. An open source software package implementing our method is available from https://github.com/kr-colab/mapNN.

Indexed as

Genetics, PopulationNeural Networks, ComputerPolymorphism, Single NucleotideAnimalsDemographyGenotypePopulation DensityWolvesconservation geneticsecological geneticsmachine learningpopulation geneticswildlife management

Identifiers

PMID39152666
PMCPMC12276964

What OpenQuestion holds

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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.