Calibrated Identification of Feature Dependencies in Single-cell Multiomics
Boyeau, P.; Bates, S.; Ergen, C.; Jordan, M.; Yosef, N.
Show abstract
Data-driven identification of functional relationships between cellular properties is an exciting promise of single-cell genomics, especially given the increasing prevalence of assays for multiomic and spatial transcriptomic analysis. Major challenges include dealing with technical factors that might introduce or obscure dependencies between measurements, handling complex generative processes that require nonlinear modeling, and correctly assessing the statistical significance of discoveries. VI-VS (Variational Inference for Variable Selection) is a comprehensive framework designed to strike a balance between robustness and interpretability. VI-VS employs nonlinear generative models to identify conditionally dependent features, all while maintaining control over false discovery rates. These conditional dependencies are more stringent and more likely to represent genuine causal relationships. VI-VS is openly available at https://github.com/YosefLab/VIVS, offering a no-compromise solution for identifying relevant feature relationships in multiomic data, advancing our understanding of molecular biology.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- GoM DE: interpreting structure in sequence count data with differential expression analysis allowing for grades of membership 97%
- scINSIGHT for interpreting single-cell gene expression from biologically heterogeneous data 97%
- Vireo: Bayesian demultiplexing of pooled single-cell RNA-seq data without genotype reference 97%
Similar papers in this journal
- Automated assignment of cell identity from single-cell multiplexed imaging and proteomic data 97%
- Belayer: Modeling discrete and continuous spatial variation in gene expression from spatially resolved transcriptomics 96%
- scCausalVI disentangles single-cell perturbation responses with causality-aware generative model 96%
Similar papers in this journal
Similar papers in this journal
- FastCCC: A permutation-free framework for scalable, robust, and reference-based cell-cell communication analysis in single cell transcriptomics studies 97%
- Normalisr: normalization and association testing for single-cell CRISPR screen and co-expression 97%
- multiDGD: A versatile deep generative model for multi-omics data 97%
Similar papers in this journal
- Randomized Spatial PCA (RASP): a computationally efficient method for dimensionality reduction of high-resolution spatial transcriptomics data 96%
- A Bayesian method to infer copy number clones from single-cell RNA and ATAC sequencing 96%
- Trajectory inference from single-cell genomics data with a process time model 96%
"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.