Evidence map›Paper›PMID 39185244›Full record

ArticlebioRxiv : the preprint server for biology2024

Tree sequences as a general-purpose tool for population genetic inference.

Logan S Whitehouse, Dylan Ray, Daniel R Schrider

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Logan S WhitehouseDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA, 120 Mason Farm Rd, Chapel Hill, NC 27514.ORCID 0000-0002-5771-1503
Dylan RayDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA, 120 Mason Farm Rd, Chapel Hill, NC 27514.
Daniel R SchriderDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina, USA, 120 Mason Farm Rd, Chapel Hill, NC 27514.ORCID 0000-0001-5249-4151

Funding

Deep learning for population geneticsR01HG010774 · NHGRI · UNIVERSITY OF OREGON · PI ANDREW D KERN · 2020 to 2026
$3.2M
The evolution of virulence in the fungal pathogen HistoplasmaR01AI153523 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MATUTE, DANIEL · 2021 to 2025
$3.2M
Advancing evolutionary genetics through deep learningR35GM138286 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DANIEL R SCHRIDER · 2020 to 2026
$2.8M
NHGRI NIH HHS R01 HG010774NIAID NIH HHS R01 AI153523NIGMS NIH HHS R35 GM138286
6 · The paper itself

Abstract

As population genetics data increases in size new methods have been developed to store genetic information in efficient ways, such as tree sequences. These data structures are computationally and storage efficient, but are not interchangeable with existing data structures used for many population genetic inference methodologies such as the use of convolutional neural networks (CNNs) applied to population genetic alignments. To better utilize these new data structures we propose and implement a graph convolutional network (GCN) to directly learn from tree sequence topology and node data, allowing for the use of neural network applications without an intermediate step of converting tree sequences to population genetic alignment format. We then compare our approach to standard CNN approaches on a set of previously defined benchmarking tasks including recombination rate estimation, positive selection detection, introgression detection, and demographic model parameter inference. We show that tree sequences can be directly learned from using a GCN approach and can be used to perform well on these common population genetics inference tasks with accuracies roughly matching or even exceeding that of a CNN-based method. As tree sequences become more widely used in population genetics research we foresee developments and optimizations of this work to provide a foundation for population genetics inference moving forward.

Indexed as

ancestral recombination graphsdemographic inferenceintrogressionrecombination rate estimationselective sweepstree sequences

Identifiers

PMID39185244
PMCPMC11343121

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.