Evidence map›Paper›PMID 27824859›Full record

ArticlePLoS genetics2016

The Strength of Selection against Neanderthal Introgression.

Ivan Juric, Simon Aeschbacher, Graham Coop

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers.

0numbers the graph read from it
0cells of the map it votes in
162citing 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

162 citing papers in PubMed.

  1. Trial
  2. Genetics and genomics of hybridization.Nature reviews. Genetics · 2026
    Review
  3. Article
  4. A tsunami of genome reshuffling.Nature ecology & evolution · 2026
    Article
  5. Review
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  18. Review
  19. Article
  20. Article

102 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

3 authors.

Ivan JuricCenter for Population Biology, University of California, Davis, California, United States of America.
Simon AeschbacherCenter for Population Biology, University of California, Davis, California, United States of America.
Graham CoopCenter for Population Biology, University of California, Davis, California, United States of America.ORCID http://orcid.org/0000-0001-8431-0302

Funding

Genome-wide approaches to polygenic adaptationR01GM108779 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COOP, GRAHAM · 2014 to 2019
$1.0M
NIGMS NIH HHS R01 GM108779
6 · The paper itself

Abstract

Hybridization between humans and Neanderthals has resulted in a low level of Neanderthal ancestry scattered across the genomes of many modern-day humans. After hybridization, on average, selection appears to have removed Neanderthal alleles from the human population. Quantifying the strength and causes of this selection against Neanderthal ancestry is key to understanding our relationship to Neanderthals and, more broadly, how populations remain distinct after secondary contact. Here, we develop a novel method for estimating the genome-wide average strength of selection and the density of selected sites using estimates of Neanderthal allele frequency along the genomes of modern-day humans. We confirm that East Asians had somewhat higher initial levels of Neanderthal ancestry than Europeans even after accounting for selection. We find that the bulk of purifying selection against Neanderthal ancestry is best understood as acting on many weakly deleterious alleles. We propose that the majority of these alleles were effectively neutral-and segregating at high frequency-in Neanderthals, but became selected against after entering human populations of much larger effective size. While individually of small effect, these alleles potentially imposed a heavy genetic load on the early-generation human-Neanderthal hybrids. This work suggests that differences in effective population size may play a far more important role in shaping levels of introgression than previously thought.

Indexed as

Genetics, PopulationGenome, HumanAllelesAnimalsAsian PeopleGene FrequencyHaplotypesHumansHybridization, GeneticNeanderthalsPhylogenyPolymorphism, Single NucleotideSelection, GeneticWhite People

Identifiers

PMID27824859
PMCPMC5100956

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Read underepoch 390

Registered trials

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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.