Evidence map›Paper›PMID 38775680›Full record

ArticleBioinformatics (Oxford, England)2024

Computing linkage disequilibrium aware genome embeddings using autoencoders.

Gizem Taş, Timo Westerdijk, Eric Postma, Project MinE ALS GWAS Consortium, Jan H Veldink, Alexander Schönhuth, Marleen Balvert

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Gizem TaşDepartment of Econometrics and Operations Research, Tilburg University, Tilburg 5037AB, The Netherlands.ORCID 0009-0008-2409-0246
Timo WesterdijkDepartment of Neurology, University Medical Center Utrecht, Utrecht 3584CX, The Netherlands.
Eric PostmaDepartment of Cognitive Science and Artificial Intelligence, Tilburg University, Tilburg 5037AB, The Netherlands.
Project MinE ALS GWAS Consortium
Jan H VeldinkDepartment of Neurology, University Medical Center Utrecht, Utrecht 3584CX, The Netherlands.ORCID 0000-0001-5572-9657
Alexander SchönhuthFaculty of Technology, Bielefeld University, Bielefeld 33615, Germany.ORCID 0000-0003-3529-0856
Marleen BalvertDepartment of Econometrics and Operations Research, Tilburg University, Tilburg 5037AB, The Netherlands.ORCID 0000-0002-2376-9301

Funding

Dutch ALS Foundation AV20190010
6 · The paper itself

Abstract

motivationThe completion of the genome has paved the way for genome-wide association studies (GWAS), which explained certain proportions of heritability. GWAS are not optimally suited to detect non-linear effects in disease risk, possibly hidden in non-additive interactions (epistasis). Alternative methods for epistasis detection using, e.g. deep neural networks (DNNs) are currently under active development. However, DNNs are constrained by finite computational resources, which can be rapidly depleted due to increasing complexity with the sheer size of the genome. Besides, the curse of dimensionality complicates the task of capturing meaningful genetic patterns for DNNs; therefore necessitates dimensionality reduction.

resultsWe propose a method to compress single nucleotide polymorphism (SNP) data, while leveraging the linkage disequilibrium (LD) structure and preserving potential epistasis. This method involves clustering correlated SNPs into haplotype blocks and training per-block autoencoders to learn a compressed representation of the block's genetic content. We provide an adjustable autoencoder design to accommodate diverse blocks and bypass extensive hyperparameter tuning. We applied this method to genotyping data from Project MinE, and achieved 99% average test reconstruction accuracy-i.e. minimal information loss-while compressing the input to nearly 10% of the original size. We demonstrate that haplotype-block based autoencoders outperform linear Principal Component Analysis (PCA) by approximately 3% chromosome-wide accuracy of reconstructed variants. To the extent of our knowledge, our approach is the first to simultaneously leverage haplotype structure and DNNs for dimensionality reduction of genetic data. AVAILABILITY AND IMPLEMENTATION: Data are available for academic use through Project MinE at https://www.projectmine.com/research/data-sharing/, contingent upon terms and requirements specified by the source studies. Code is available at https://github.com/gizem-tas/haploblock-autoencoders.

Indexed as

Genome-Wide Association StudyLinkage DisequilibriumPolymorphism, Single NucleotideAlgorithmsEpistasis, GeneticHaplotypesHumansNeural Networks, Computer

Identifiers

PMID38775680
PMCPMC11208726

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.