Multivariate Random Forests for Cross-Modal Multi-Omics Integration
Zhang, W.; Wang, L.; Franzmann, E. J.; Chen, X. S.
Show abstract
Multi-omics studies are widely used across many areas of biomedical research. In many diseases, some signals are shared across data types, while others are strongest in a single omics layer. Current multi-omics clustering methods often either merge all data types into a single representation, which can blur biology that is strong in one layer, or rely on linear structure that may miss more complex relationships across data types. We introduce O_SCPLOWMULTIC_SCPLOWRF, a random-forest-based method that handles complex data types and separates shared and modality-specific structure for multi-omics data. O_SCPLOWMULTIC_SCPLOWRF learns sample similarities across omics layers from multivariate random forests, combines them across data types, and uses the resulting weights to estimate the part of each omics layer that is predictable from the others. The remaining residual is treated as modality-specific signal, allowing shared and modality-specific similarities to be clustered separately. In simulations, O_SCPLOWMULTIC_SCPLOWRF recovered shared clusters as well as or better than established integrative methods while more reliably separating modality-specific signal under nonlinear data structures. In TCGA head and neck squamous cell carcinoma, the shared component aligned with the main subtype structure across established reference classifications, while gene- and miRNA-specific components revealed additional immune and developmental biology. In the ADNI cohort with matched blood DNA methylation and structural MRI, the shared cross-modal aging signal was associated with future conversion to mild cognitive impairment or Alzheimers disease, and a DNAm-specific residual signal showed exploratory additional information. These results show that O_SCPLOWMULTIC_SCPLOWRF can recover a common disease axis while retaining biologically meaningful signals specific to one data type. O_SCPLOWMULTIC_SCPLOWRF is available as an open-source R package at https://github.com/novawz/multiRF.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- scCross: A Deep Generative Model for Unifying Single-cell Multi-omics with Seamless Integration, Cross-modal Generation, and In-silico Exploration 95%
- Cross-species imputation and comparison of single-cell transcriptomic profiles 95%
- Neighborhood nonnegative matrix factorization identifies patterns and spatially-variable genes in large-scale spatial transcriptomics data 94%
Similar papers in this journal
- An in-depth comparison of linear and non-linear joint embedding methods for bulk and single-cell multi-omics 96%
- SpaTM: Topic Models for Inferring Spatially Informed Transcriptional Programs 95%
- SHEST: Single-cell-level artificial intelligence from haematoxylin and eosin morphology for cell type prediction and spatial transcriptomics reconstruction 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.