Evidence map›Paper›PMID 36788253›Full record

ArticleScientific reports2023

Hybrid autoencoder with orthogonal latent space for robust population structure inference.

Meng Yuan, Hanne Hoskens, Seppe Goovaerts, Noah Herrick, Mark D Shriver, Susan Walsh, Peter Claes

Abstract read
In one paragraph

Article in Scientific reports, 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Meng YuanDepartment of Electrical Engineering, ESAT/PSI, KU Leuven, Leuven, Belgium. meng.yuan@kuleuven.be.
Hanne HoskensDepartment of Human Genetics, KU Leuven, Leuven, Belgium.
Seppe GoovaertsDepartment of Human Genetics, KU Leuven, Leuven, Belgium.
Noah HerrickDepartment of Biology, Indiana University Purdue University Indianapolis, Indianapolis, IN, USA.
Mark D ShriverDepartment of Anthropology, Pennsylvania State University, State College, PA, USA.
Susan WalshDepartment of Biology, Indiana University Purdue University Indianapolis, Indianapolis, IN, USA.
Peter ClaesDepartment of Electrical Engineering, ESAT/PSI, KU Leuven, Leuven, Belgium. peter.claes@kuleuven.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analysis of population structure and genomic ancestry remains an important topic in human genetics and bioinformatics. Commonly used methods require high-quality genotype data to ensure accurate inference. However, in practice, laboratory artifacts and outliers are often present in the data. Moreover, existing methods are typically affected by the presence of related individuals in the dataset. In this work, we propose a novel hybrid method, called SAE-IBS, which combines the strengths of traditional matrix decomposition-based (e.g., principal component analysis) and more recent neural network-based (e.g., autoencoders) solutions. Namely, it yields an orthogonal latent space enhancing dimensionality selection while learning non-linear transformations. The proposed approach achieves higher accuracy than existing methods for projecting poor quality target samples (genotyping errors and missing data) onto a reference ancestry space and generates a robust ancestry space in the presence of relatedness. We introduce a new approach and an accompanying open-source program for robust ancestry inference in the presence of missing data, genotyping errors, and relatedness. The obtained ancestry space allows for non-linear projections and exhibits orthogonality with clearly separable population groups.

Indexed as

Genetics, PopulationNeural Networks, ComputerGenotypeHumansPrincipal Component Analysis

Identifiers

PMID36788253
PMCPMC9929087

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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.