Species-agnostic transfer learning for cross-species transcriptomics data integration without gene orthology.
Youngjun ParkNils P MuttrayAnne-Christin HauschildPublished in: Briefings in bioinformatics (2024)
Novel hypotheses in biomedical research are often developed or validated in model organisms such as mice and zebrafish and thus play a crucial role. However, due to biological differences between species, translating these findings into human applications remains challenging. Moreover, commonly used orthologous gene information is often incomplete and entails a significant information loss during gene-id conversion. To address these issues, we present a novel methodology for species-agnostic transfer learning with heterogeneous domain adaptation. We extended the cross-domain structure-preserving projection toward out-of-sample prediction. Our approach not only allows knowledge integration and translation across various species without relying on gene orthology but also identifies similar GO among the most influential genes composing the latent space for integration. Subsequently, during the alignment of latent spaces, each composed of species-specific genes, it is possible to identify functional annotations of genes missing from public orthology databases. We evaluated our approach with four different single-cell sequencing datasets focusing on cell-type prediction and compared it against related machine-learning approaches. In summary, the developed model outperforms related methods working without prior knowledge when predicting unseen cell types based on other species' data. The results demonstrate that our novel approach allows knowledge transfer beyond species barriers without the dependency on known gene orthology but utilizing the entire gene sets.
Keyphrases
- genome wide
- genome wide identification
- single cell
- copy number
- healthcare
- machine learning
- genome wide analysis
- rna seq
- big data
- type diabetes
- genetic diversity
- endothelial cells
- emergency department
- magnetic resonance imaging
- mesenchymal stem cells
- magnetic resonance
- bone marrow
- computed tomography
- electronic health record
- adipose tissue
- insulin resistance
- multidrug resistant
- metabolic syndrome
- skeletal muscle
- social media