Evidence map›Paper›PMID 36759699›Full record

ArticleG3 (Bethesda, Md.)2023

The effect of mutation subtypes on the allele frequency spectrum and population genetics inference.

Kevin Liao, Jedidiah Carlson, Sebastian Zöllner

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 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. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Kevin LiaoDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.
Jedidiah CarlsonDepartment of Integrative Biology, University of Texas at Austin, Austin, TX 78712, USA.
Sebastian ZöllnerDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.

Funding

University of Michigan Training Program in Genomic ScienceT32HG000040 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Sebastian Zoellner · 1995 to 2026
$16.4M
Population genetics for large-scale sequencing studies of diverse populationsR01HG005855 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Noah Rosenberg, Paul A Scheet · 2010 to 2026
$5.8M
Whole Genome Sequencing for Schizophrenia and Bipolar Disorder in the GPCU01MH105653 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOEHNKE, MICHAEL L · 2014 to 2018
$2.8M
1/2-Whole Genome and Exome Sequencing for Bipolar DisorderR01MH094145 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOEHNKE, MICHAEL L · 2011 to 2013
$2.0M
High-resolution map of human germline mutation patterns and inference of mutagenic mechanismsR01GM118928 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, JUN, ZOELLNER, SEBASTIAN · 2016 to 2019
$1.2M
NHGRI NIH HHS R01 HG005855NHGRI NIH HHS T32 HG000040NIGMS NIH HHS R01 GM118928NIMH NIH HHS R01 MH094145NIMH NIH HHS U01 MH105653
6 · The paper itself

Abstract

Population genetics has adapted as technological advances in next-generation sequencing have resulted in an exponential increase of genetic data. A common approach to efficiently analyze genetic variation present in large sequencing data is through the allele frequency spectrum, defined as the distribution of allele frequencies in a sample. While the frequency spectrum serves to summarize patterns of genetic variation, it implicitly assumes mutation types (A→C vs C→T) as interchangeable. However, mutations of different types arise and spread due to spatial and temporal variation in forces such as mutation rate and biased gene conversion that result in heterogeneity in the distribution of allele frequencies across sites. In this work, we explore the impact of this simplification on multiple aspects of population genetic modeling. As a site's mutation rate is strongly affected by flanking nucleotides, we defined a mutation subtype by the base pair change and adjacent nucleotides (e.g. AAA→ATA) and systematically assessed the heterogeneity in the frequency spectrum across 96 distinct 3-mer mutation subtypes using n = 3556 whole-genome sequenced individuals of European ancestry. We observed substantial variation across the subtype-specific frequency spectra, with some of the variation being influenced by molecular factors previously identified for single base mutation types. Estimates of model parameters from demographic inference performed for each mutation subtype's AFS individually varied drastically across the 96 subtypes. In local patterns of variation, a combination of regional subtype composition and local genomic factors shaped the regional frequency spectrum across genomic regions. Our results illustrate how treating variants in large sequencing samples as interchangeable may confound population genetic frameworks and encourages us to consider the unique evolutionary mechanisms of analyzed polymorphisms.

Indexed as

Genetics, PopulationMutation RateGene FrequencyHumansMutationNucleotidesNucleotidesallele frequency spectrummutation typespopulation genetics

Identifiers

PMID36759699
PMCPMC10085755

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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.