Evidence map›Paper›PMID 22022285›Full record

ArticlePLoS genetics2011

Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome.

Kirk E Lohmueller, Anders Albrechtsen, Yingrui Li, Su Yeon Kim, Thorfinn Korneliussen, Nicolas Vinckenbosch, Geng Tian, Emilia Huerta-Sanchez, Alison F Feder, Niels Grarup and 10 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
9.6field-weighted citation impact, top 2% of its field
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

95 citing papers in PubMed, 179 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. A model for background selection in non-equilibrium populations.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

35 more citing papers are in PubMed but not listed here.

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

20 authors at 10 institutions in 4 countries.

Kirk E LohmuellerDepartment of Integrative Biology, University of California Berkeley, Berkeley, California, United States of America. k.lohmueller@berkeley.edu
Anders Albrechtsen
Yingrui Li
Su Yeon Kim
Thorfinn Korneliussen
Nicolas Vinckenbosch
Geng Tian
Emilia Huerta-Sanchez
Alison F Feder
Niels Grarup
Torben Jørgensen
Tao Jiang
Daniel R Witte
Annelli Sandbæk
Ines Hellmann
Torsten Lauritzen
Torben Hansen
Oluf Pedersen
Jun Wang
Rasmus Nielsen
University of California, Berkeley · USNovo Nordisk Foundation · DKAarhus University · DKBGI Group (China) · CNUniversity of Copenhagen · DKBeijing Institute of Genomics · CNGlostrup Hospital · DKSteno Diabetes Center · DKUniversity of Pennsylvania · USUniversity of Vienna · AT

Funding

Population Genetic Inferences From Dense Genotype DataR01HG003229 · NHGRI · CORNELL UNIVERSITY ITHACA · PI BUSTAMANTE, CARLOS DANIEL, CLARK, ANDREW G · 2004 to 2013
$4.8M
Population genetics of deleterious polymorphism in human populationsF32HG005308 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI LOHMUELLER, KIRK · 2009 to 2009
$23k
NHGRI NIH HHS F32 HG005308NHGRI NIH HHS F32HG005308NHGRI NIH HHS R01 HG003229
6 · The paper itself

Abstract

A major question in evolutionary biology is how natural selection has shaped patterns of genetic variation across the human genome. Previous work has documented a reduction in genetic diversity in regions of the genome with low recombination rates. However, it is unclear whether other summaries of genetic variation, like allele frequencies, are also correlated with recombination rate and whether these correlations can be explained solely by negative selection against deleterious mutations or whether positive selection acting on favorable alleles is also required. Here we attempt to address these questions by analyzing three different genome-wide resequencing datasets from European individuals. We document several significant correlations between different genomic features. In particular, we find that average minor allele frequency and diversity are reduced in regions of low recombination and that human diversity, human-chimp divergence, and average minor allele frequency are reduced near genes. Population genetic simulations show that either positive natural selection acting on favorable mutations or negative natural selection acting against deleterious mutations can explain these correlations. However, models with strong positive selection on nonsynonymous mutations and little negative selection predict a stronger negative correlation between neutral diversity and nonsynonymous divergence than observed in the actual data, supporting the importance of negative, rather than positive, selection throughout the genome. Further, we show that the widespread presence of weakly deleterious alleles, rather than a small number of strongly positively selected mutations, is responsible for the correlation between neutral genetic diversity and recombination rate. This work suggests that natural selection has affected multiple aspects of linked neutral variation throughout the human genome and that positive selection is not required to explain these observations.

Indexed as

Genetic DriftGenome, HumanRecombination, GeneticAnimalsEvolution, MolecularGene FrequencyGenetic VariationHumansModels, GeneticMutationPan troglodytesPopulationSelection, Genetic

Identifiers

PMID22022285
PMCPMC3192825
OpenAlexW2103677370

What OpenQuestion holds

Textmetadata
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.