bioRxiv Science⌕ Search

bioRxiv · 10.1101/592089

Modeling latent flows on single-cell data using the Hodge decomposition

Abstract

Single-cell analysis is a powerful technique used to identify a specific cell population of interest during differentiation, aging, or oncogenesis. Individual cells occupy a particular transient state in the cell cycle, circadian rhythm, or during cell death. An appealing concept of pseudo-time trajectory analysis of single-cell RNA sequencing data was proposed in the software Monocle, and several methods of trajectory analysis have since been published to date. These aim to infer the ordering of cells and enable the tracing of gene expression profile trajectories in cell differentiation and reprogramming. However, the methods are restricted in terms of time structure because of the pre-specified structure of trajectories (linear, branched, tree or cyclic) which contrasts with the mixed state of single cells.\n\nHere, we propose a technique to extract underlying flows in single-cell data based on the Hodge decomposition (HD). HD is a theorem of vector fields on a manifold which guarantees that any given flow can decompose into three types of orthogonal component: gradient-flow (acyclic), curl-, and harmonic-flow (cyclic). HD is generalized on a simplicial complex (graph) and the discretized HD has only a weak assumption that the graph is directed. Therefore, in principle, HD can extract flows from any mixture of tree and cyclic time flows of observed cells. The decomposed flows provide intuitive interpretations about complex flow because of their linearity and orthogonality. Thus, each extracted flow can be focused on separately with no need to consider crosstalk.\n\nWe developed ddhodge software, which aims to model the underlying flow structure that implies unobserved time or causal relations in the hodge-podge collection of data points. We demonstrated that the mathematical framework of HD is suitable to reconstruct a sparse graph representation of diffusion process as a candidate model of differentiation while preserving the divergence of the original fully-connected graph. The preserved divergence can be used as an indicator of the source and sink cells in the observed population. A sparse graph representation of the diffusion process transforms data analysis of the non-linear structure embedded in the high-dimensional space of single-cell data into inspection of the visible flow using graph algorithms. Hence, ddhodge is a suitable toolkit to visualize, inspect, and subsequently interpret large data sets including, but not limited to, high-throughput measurements of biological data.\n\nThe beta version of ddhodge R package is available at: https://github.com/kazumits/ddhodge

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Maehara, K., Ohkawa, Y.. 2019-03-28. Modeling latent flows on single-cell data using the Hodge decomposition. https://doi.org/10.1101/592089

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Deducing splicing events from transcript sets with splicelogic

Long-read RNA sequencing captures a greater proportion of full-length transcripts, enabling more accurate isoform identification, discovery of novel isoforms, and more precise differential transcript usage analysis. However, comparing transcripts, whether between conditions or between sets such as novel and annotated isoforms, yields complex isoform changes that are hard to manipulate, summarize, and visualize. This is compounded by vertical integration of some tools, where downstream analysis depends on the specific output of a particular upstream tool. To address this gap, we have developed splicelogic, an R/Bioconductor package that makes transcript-set comparisons biologically interpretable by turning them into discrete splicing events, such as exon skipping, alternative splice sites, intron retention, and alternative transcription start and end sites. We designed splicelogic to integrate easily with existing RNA-seq workflows and tools. The splicelogic functions are modular, readable, and extensible, making it easy for users to adapt core logic to their own custom scientific questions or novel splicing definitions. By obtaining interpretable splicing events from transcript changes, splicelogic enables downstream analyses, including annotation of RNA-binding protein recognition sites, alongside summary statistics and visualization. The splicelogic package is publicly available and distributed through Bioconductor.

bioinformatics↗

Contrastive Learning Improves Generalization on M2OR Olfactory Binding Dataset

Olfaction-based biosensors stand to have profound impacts in fields such as medical diagnostics, national security, and drug discovery. A promising mode of vapor phase biodetection mimics volatile organic compound-olfactory receptor (VOC-OR) interactions with target-specific protein or peptide probes; however, lack of experimental coverage remains a core bottleneck. Current computational approaches aim to improve prediction of VOC-OR binding to reduce experimental burden, and current machine learning approaches fail to demonstrate a level of generalization that addresses current engineering challenges. Here, using the Molecular to Olfactory Dataset (M2OR) and Insect Olfactory Binding Protein Database (iOBPdb) datasets, data partitioning methods and their performance are evaluated on a neural network and contrastive learning framework on such VOC-OR binding datasets, varying: model training, architecture, and structure of the input data distribution. It was found that holding out certain chemical or proteomic motifs from the training data diminished model performance with a two layer neural network model. The model was able to generalize to state of the art performance (0.88 AUCROC) on every data split by applying a contrastive learning objective defined by shared molecular constituents and a stochastic sampler. This suggests the contrastive objective provides a strong inductive bias for neural networks to predict novel VOC-OR pairs. These findings highlight that model performance on pairwise biological interaction datasets can be inflated through identity leakage from constituent overlap, and emphasize the need for more robust evaluation protocols. Furthermore, we show contrastive regularization mitigates dataset degeneracy through enforcement of compatibility in the models latent geometry that may extend to other binder target-datasets where identity leakage confounds evaluation.

bioinformatics↗

Plate design confounds donor variation and model evaluation in single-cell perturbation screens

Single-cell screens of immune cells from many donors are used to study why individuals respond differently and to benchmark response models. Each donor-perturbation combination typically occupies one well, controls are grouped, and donors share one layout, so technical effects can look biological. Using a 90-cytokine screen, two compound screens, four cohorts and simulations, we show that well effects explain most replicate-control variation in abundant cell types, controls carry a shared offset, and identical control wells differ by hundreds of differentially expressed genes at a standard threshold, about as many as two receptor-negative proteins do. Negative controls, design-aware estimators and perturbation-specific evaluation change the interpretation of four recent analyses. A deep-learning model that scores below a perturbation-agnostic predictor under standard evaluation outperforms a simple baseline on perturbation-specific differences in two of three cell types (significantly in one with stricter controls), but predicts less well the component shared with inert wells.

bioinformatics↗