Evidence map›Paper›PMID 36947126›Full record

ArticleMolecular biology and evolution2023

Localizing Post-Admixture Adaptive Variants with Object Detection on Ancestry-Painted Chromosomes.

Iman Hamid, Katharine L Korunes, Daniel R Schrider, Amy Goldberg

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Recomb-Mix: fast and accurate local ancestry inference.Bioinformatics (Oxford, England) · 2025
    Article
  4. Article
  5. Article
  6. Digital Image Processing to Detect Adaptive Evolution.Molecular biology and evolution · 2024
    Article
  7. Fast and accurate local ancestry inference with Recomb-Mix.bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. IntroUNET: identifying introgressed alleles via semantic segmentation.bioRxiv : the preprint server for biology · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. 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

4 authors at 2 institutions in 1 country.

Iman HamidDepartment of Evolutionary Anthropology, Duke University, Durham, NC.
Katharine L KorunesDepartment of Evolutionary Anthropology, Duke University, Durham, NC.ORCID 0000-0002-2648-4707
Daniel R SchriderDepartment of Genetics, University of North Carolina, Chapel Hill, NC.ORCID 0000-0001-5249-4151
Amy GoldbergDepartment of Evolutionary Anthropology, Duke University, Durham, NC.ORCID 0000-0001-9306-1539
Duke University · USUniversity of North Carolina at Chapel Hill · US

Funding

Inferring the evolutionary history of admixed populationsR35GM133481 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Amy Goldberg · 2019 to 2026
$2.8M
Advancing evolutionary genetics through deep learningR35GM138286 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DANIEL R SCHRIDER · 2020 to 2026
$2.8M
Evolutionary Dynamics of Zoonotic MalariaR01AI175622 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Amy Goldberg · 2023 to 2026
$2.5M
Natural Selection in Admixed PopulationsF32GM139313 · NIGMS · DUKE UNIVERSITY · PI KORUNES, KATHARINE LOVE · 2020 to 2021
$114k
6 · The paper itself

Abstract

Gene flow between previously differentiated populations during the founding of an admixed or hybrid population has the potential to introduce adaptive alleles into the new population. If the adaptive allele is common in one source population, but not the other, then as the adaptive allele rises in frequency in the admixed population, genetic ancestry from the source containing the adaptive allele will increase nearby as well. Patterns of genetic ancestry have therefore been used to identify post-admixture positive selection in humans and other animals, including examples in immunity, metabolism, and animal coloration. A common method identifies regions of the genome that have local ancestry "outliers" compared with the distribution across the rest of the genome, considering each locus independently. However, we lack theoretical models for expected distributions of ancestry under various demographic scenarios, resulting in potential false positives and false negatives. Further, ancestry patterns between distant sites are often not independent. As a result, current methods tend to infer wide genomic regions containing many genes as under selection, limiting biological interpretation. Instead, we develop a deep learning object detection method applied to images generated from local ancestry-painted genomes. This approach preserves information from the surrounding genomic context and avoids potential pitfalls of user-defined summary statistics. We find the method is robust to a variety of demographic misspecifications using simulated data. Applied to human genotype data from Cabo Verde, we localize a known adaptive locus to a single narrow region compared with multiple or long windows obtained using two other ancestry-based methods.

Indexed as

Genetics, PopulationGenomicsAnimalsChromosomesGene FlowGenotypeHumansadmixtureconvolutional neural networkintrogressionobject detectionselection

Identifiers

PMID36947126
PMCPMC10116606
OpenAlexW4353015435

What Socratic 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 Socratic graph.