Your browser doesn't support javascript.
loading
Computing linkage disequilibrium aware genome embeddings using autoencoders.
Tas, Gizem; Westerdijk, Timo; Postma, Eric; Veldink, Jan H; Schönhuth, Alexander; Balvert, Marleen.
Afiliação
  • Tas G; Department of Econometrics and Operations Research, Tilburg University, Tilburg 5037AB, The Netherlands.
  • Westerdijk T; Department of Neurology, University Medical Center Utrecht, Utrecht 3584CX, The Netherlands.
  • Postma E; Department of Cognitive Science and Artificial Intelligence, Tilburg University, Tilburg 5037AB, The Netherlands.
  • Veldink JH; Department of Neurology, University Medical Center Utrecht, Utrecht 3584CX, The Netherlands.
  • Schönhuth A; Faculty of Technology, Bielefeld University, Bielefeld 33615, Germany.
  • Balvert M; Department of Econometrics and Operations Research, Tilburg University, Tilburg 5037AB, The Netherlands.
Bioinformatics ; 40(6)2024 06 03.
Article em En | MEDLINE | ID: mdl-38775680
ABSTRACT
MOTIVATION The 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.

RESULTS:

We 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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Desequilíbrio de Ligação / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Limite: Humans Idioma: En Revista: Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Desequilíbrio de Ligação / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Limite: Humans Idioma: En Revista: Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda