Evidence map›Paper›PMID 36124792›Full record

ArticleBioinformatics (Oxford, England)2022

SALAI-Net: species-agnostic local ancestry inference network.

Benet Oriol Sabat, Daniel Mas Montserrat, Xavier Giro-I-Nieto, Alexander G Ioannidis

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Recomb-Mix: fast and accurate local ancestry inference.Bioinformatics (Oxford, England) · 2025
    Article
  6. Review
  7. Old vs. New Local Ancestry Inference in HCHS/SOL: A Comparative Study.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Fast and accurate local ancestry inference with Recomb-Mix.bioRxiv : the preprint server for biology · 2024
    Article
  11. Machine Learning Strategies for Improved Phenotype Prediction in Underrepresented Populations.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2024
    Article
  12. Review
  13. Article
  14. Neural ADMIXTURE for rapid genomic clustering.Nature computational science · 2023
    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.

Benet Oriol SabatDepartment of Signal Theory and Communications, Universitat Politecnica de Catalunya, Barcelona 08034, Spain.
Daniel Mas MontserratDepartment of Biomedical Data Science, Stanford Medical School.
Xavier Giro-I-NietoDepartment of Signal Theory and Communications, Universitat Politecnica de Catalunya, Barcelona 08034, Spain.
Alexander G IoannidisDepartment of Biomedical Data Science, Stanford Medical School.

Funding

SOFTWARE FOR LARGE-SCALE INFERENCE OF THE GENETICS OF LIFESTYLE MEASURES, BIOMARKERS, AND COMMON AND RARE DISEASESR01HG010140 · NHGRI · STANFORD UNIVERSITY · PI KUNDAJE, ANSHUL, MONTGOMERY, STEPHEN · 2018 to 2022
$2.0M
NHGRI NIH HHS R01 HG010140
6 · The paper itself

Abstract

motivationLocal ancestry inference (LAI) is the high resolution prediction of ancestry labels along a DNA sequence. LAI is important in the study of human history and migrations, and it is beginning to play a role in precision medicine applications including ancestry-adjusted genome-wide association studies (GWASs) and polygenic risk scores (PRSs). Existing LAI models do not generalize well between species, chromosomes or even ancestry groups, requiring re-training for each different setting. Furthermore, such methods can lack interpretability, which is an important element in each of these applications.

resultsWe present SALAI-Net, a portable statistical LAI method that can be applied on any set of species and ancestries (species-agnostic), requiring only haplotype data and no other biological parameters. Inspired by identity by descent methods, SALAI-Net estimates population labels for each segment of DNA by performing a reference matching approach, which leads to an interpretable and fast technique. We benchmark our models on whole-genome data of humans and we test these models' ability to generalize to dog breeds when trained on human data. SALAI-Net outperforms previous methods in terms of balanced accuracy, while generalizing between different settings, species and datasets. Moreover, it is up to two orders of magnitude faster and uses considerably less RAM memory than competing methods. AVAILABILITY AND IMPLEMENTATION: We provide an open source implementation and links to publicly available data at github.com/AI-sandbox/SALAI-Net. Data is publicly available as follows: https://www.internationalgenome.org (1000 Genomes), https://www.simonsfoundation.org/simons-genome-diversity-project (Simons Genome Diversity Project), https://www.sanger.ac.uk/resources/downloads/human/hapmap3.html (HapMap), ftp://ngs.sanger.ac.uk/production/hgdp/hgdp_wgs.20190516 (Human Genome Diversity Project) and https://www.ncbi.nlm.nih.gov/bioproject/PRJNA448733 (Canid genomes). SUPPLEMENTARY INFORMATION: Supplementary data are available from Bioinformatics online.

Indexed as

Genome-Wide Association StudyAnimalsDogsHaplotypesHumans

Identifiers

PMID36124792
PMCPMC9486591

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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.