Evidence map›Paper›PMID 37873208›Full record

ArticlebioRxiv : the preprint server for biology2023

A likelihood-based framework for demographic inference from genealogical trees.

Caoqi Fan, Jordan L Cahoon, Bryan L Dinh, Diego Ortega-Del Vecchyo, Christian Huber, Michael D Edge, Nicholas Mancuso, Charleston W K Chiang

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Caoqi FanDepartment of Quantitative and Computational Biology, University of Southern California.
Jordan L CahoonDepartment of Quantitative and Computational Biology, University of Southern California.
Bryan L DinhDepartment of Quantitative and Computational Biology, University of Southern California.
Diego Ortega-Del VecchyoLaboratorio Internacional de Investigación sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, Querétaro, México.
Christian HuberDepartment of Biology, Penn State University, University Park, PA, USA.
Michael D EdgeDepartment of Quantitative and Computational Biology, University of Southern California.
Nicholas MancusoDepartment of Quantitative and Computational Biology, University of Southern California.
Charleston W K ChiangDepartment of Quantitative and Computational Biology, University of Southern California.

Funding

Leveraging the Evolutionary History to Improve Identification of Trait-Associated Alleles and Risk Stratification Models in Native HawaiiansR01HG011646 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Charleston Chiang · 2022 to 2026
$4.0M
Traits on trees: Population genomics for understanding complex phenotypesR35GM137758 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Michael Donald Edge · 2020 to 2026
$2.5M
An evolutionary framework to elucidate and interpret the genetic architecture of complex traits in diverse populations - diversity supplementR35GM142783 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIANG, CHARLESTON · 2021 to 2025
$2.2M
A genome-wide genealogical framework for statistical and population genetic analysisR01HG012605 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Charleston Chiang · 2023 to 2026
$2.1M
NHGRI NIH HHS R01 HG011646NHGRI NIH HHS R01 HG012605NIGMS NIH HHS R35 GM137758NIGMS NIH HHS R35 GM142783
6 · The paper itself

Abstract

The demographic history of a population drives the pattern of genetic variation and is encoded in the gene-genealogical trees of the sampled alleles. However, existing methods to infer demographic history from genetic data tend to use relatively low-dimensional summaries of the genealogy, such as allele frequency spectra. As a step toward capturing more of the information encoded in the genome-wide sequence of genealogical trees, here we propose a novel framework called the genealogical likelihood (gLike), which derives the full likelihood of a genealogical tree under any hypothesized demographic history. Employing a graph-based structure, gLike summarizes across independent trees the relationships among all lineages in a tree with all possible trajectories of population memberships through time and efficiently computes the exact marginal probability under a parameterized demographic model. Through extensive simulations and empirical applications on populations that have experienced multiple admixtures, we showed that gLike can accurately estimate dozens of demographic parameters when the true genealogy is known, including ancestral population sizes, admixture timing, and admixture proportions. Moreover, when using genealogical trees inferred from genetic data, we showed that gLike outperformed conventional demographic inference methods that leverage only the allele-frequency spectrum and yielded parameter estimates that align with established historical knowledge of the past demographic histories for populations like Latino Americans and Native Hawaiians. Furthermore, our framework can trace ancestral histories by analyzing a sample from the admixed population without proxies for its source populations, removing the need to sample ancestral populations that may no longer exist. Taken together, our proposed gLike framework harnesses underutilized genealogical information to offer exceptional sensitivity and accuracy in inferring complex demographies for humans and other species, particularly as estimation of genome-wide genealogies improves.

Identifiers

PMID37873208
PMCPMC10592779

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.