Evidence map›Paper›PMID 39847470›Full record

ArticleMolecular biology and evolution2025

Modeling Biases from Low-Pass Genome Sequencing to Enable Accurate Population Genetic Inferences.

Emanuel M Fonseca, Linh N Tran, Hannah Mendoza, Ryan N Gutenkunst

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

The trial behind it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Emanuel M FonsecaDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0002-2952-8816
Linh N TranDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0003-0574-0887
Hannah MendozaDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.
Ryan N GutenkunstDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0002-8659-0579

Funding

Joint inferences of natural selection between sites and populationsR01GM127348 · NIGMS · UNIVERSITY OF ARIZONA · PI GUTENKUNST, RYAN · 2019 to 2023
$1.7M
Population genomic inferences of history and selection across populations and timeR35GM149235 · NIGMS · UNIVERSITY OF ARIZONA · PI Ryan Gutenkunst · 2023 to 2026
$1.3M
NIGMS NIH HHS R01 GM127348NIGMS NIH HHS R35 GM149235
6 · The paper itself

Abstract

Low-pass genome sequencing is cost-effective and enables analysis of large cohorts. However, it introduces biases by reducing heterozygous genotypes and low-frequency alleles, impacting subsequent analyses such as model-based demographic history inference. Several approaches exist for inferring an unbiased allele frequency spectrum (AFS) from low-pass data, but they can introduce spurious noise into the AFS. Rather than correcting the AFS, here, we developed an approach that incorporates low-pass biases into the demographic modeling and directly analyzes the AFS from low-pass data. Our probabilistic model captures biases from the Genome Analysis Toolkit multisample calling pipeline, and we implemented it in the population genomic inference software dadi. We evaluated the model using simulated low-pass datasets and found that it alleviated low-pass biases in inferred demographic parameters. We further validated the model by downsampling 1000 Genomes Project data, demonstrating its effectiveness on real data. Our model is widely applicable and substantially improves model-based inferences from low-pass population genomic data.

Indexed as

Genetics, PopulationModels, GeneticWhole Genome SequencingGene FrequencyHumansSoftwareallele frequency spectrumdemography inferenceGATK multisample callinginbreedinglow-pass sequencing

Identifiers

PMID39847470
PMCPMC11756381

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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.