Modelling Technical and Biological Effects in scRNA-seq data with
Scalable GPLVMs
- URL: http://arxiv.org/abs/2209.06716v1
- Date: Wed, 14 Sep 2022 15:25:15 GMT
- Title: Modelling Technical and Biological Effects in scRNA-seq data with
Scalable GPLVMs
- Authors: Vidhi Lalchand, Aditya Ravuri, Emma Dann, Natsuhiko Kumasaka, Dinithi
Sumanaweera, Rik G.H. Lindeboom, Shaista Madad, Sarah A. Teichmann, Neil D.
Lawrence
- Abstract summary: We extend a popular approach for probabilistic non-linear dimensionality reduction, the Gaussian process latent variable model, to scale to massive single-cell datasets.
The key idea is to use an augmented kernel which preserves the factorisability of the lower bound allowing for fast variational inference.
- Score: 6.708052194104378
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Single-cell RNA-seq datasets are growing in size and complexity, enabling the
study of cellular composition changes in various biological/clinical contexts.
Scalable dimensionality reduction techniques are in need to disentangle
biological variation in them, while accounting for technical and biological
confounders. In this work, we extend a popular approach for probabilistic
non-linear dimensionality reduction, the Gaussian process latent variable
model, to scale to massive single-cell datasets while explicitly accounting for
technical and biological confounders. The key idea is to use an augmented
kernel which preserves the factorisability of the lower bound allowing for fast
stochastic variational inference. We demonstrate its ability to reconstruct
latent signatures of innate immunity recovered in Kumasaka et al. (2021) with
9x lower training time. We further analyze a COVID dataset and demonstrate
across a cohort of 130 individuals, that this framework enables data
integration while capturing interpretable signatures of infection.
Specifically, we explore COVID severity as a latent dimension to refine patient
stratification and capture disease-specific gene expression.
Related papers
- Generating Multi-Modal and Multi-Attribute Single-Cell Counts with CFGen [76.02070962797794]
We present Cell Flow for Generation, a flow-based conditional generative model for multi-modal single-cell counts.
Our results suggest improved recovery of crucial biological data characteristics while accounting for novel generative tasks.
arXiv Detail & Related papers (2024-07-16T14:05:03Z) - Semantically Rich Local Dataset Generation for Explainable AI in Genomics [0.716879432974126]
Black box deep learning models trained on genomic sequences excel at predicting the outcomes of different gene regulatory mechanisms.
We propose using Genetic Programming to generate datasets by evolving perturbations in sequences that contribute to their semantic diversity.
arXiv Detail & Related papers (2024-07-03T10:31:30Z) - Scalable Amortized GPLVMs for Single Cell Transcriptomics Data [9.010523724015398]
Dimensionality reduction is crucial for analyzing large-scale single-cell RNA-seq data.
We introduce an improved model, the amortized variational model (BGPLVM)
BGPLVM is tailored for single-cell RNA-seq with specialized encoder, kernel, and likelihood designs.
arXiv Detail & Related papers (2024-05-06T21:54:38Z) - Single-Cell Deep Clustering Method Assisted by Exogenous Gene
Information: A Novel Approach to Identifying Cell Types [50.55583697209676]
We develop an attention-enhanced graph autoencoder, which is designed to efficiently capture the topological features between cells.
During the clustering process, we integrated both sets of information and reconstructed the features of both cells and genes to generate a discriminative representation.
This research offers enhanced insights into the characteristics and distribution of cells, thereby laying the groundwork for early diagnosis and treatment of diseases.
arXiv Detail & Related papers (2023-11-28T09:14:55Z) - Tertiary Lymphoid Structures Generation through Graph-based Diffusion [54.37503714313661]
In this work, we leverage state-of-the-art graph-based diffusion models to generate biologically meaningful cell-graphs.
We show that the adopted graph diffusion model is able to accurately learn the distribution of cells in terms of their tertiary lymphoid structures (TLS) content.
arXiv Detail & Related papers (2023-10-10T14:37:17Z) - PhagoStat a scalable and interpretable end to end framework for
efficient quantification of cell phagocytosis in neurodegenerative disease
studies [0.0]
We introduce an end-to-end, scalable, and versatile real-time framework for quantifying and analyzing phagocytic activity.
Our proposed pipeline is able to process large data-sets and includes a data quality verification module.
We apply our pipeline to analyze microglial cell phagocytosis in FTD and obtain statistically reliable results.
arXiv Detail & Related papers (2023-04-26T18:10:35Z) - AMIGO: Sparse Multi-Modal Graph Transformer with Shared-Context
Processing for Representation Learning of Giga-pixel Images [53.29794593104923]
We present a novel concept of shared-context processing for whole slide histopathology images.
AMIGO uses the celluar graph within the tissue to provide a single representation for a patient.
We show that our model is strongly robust to missing information to an extent that it can achieve the same performance with as low as 20% of the data.
arXiv Detail & Related papers (2023-03-01T23:37:45Z) - Learning Causal Representations of Single Cells via Sparse Mechanism
Shift Modeling [3.2435888122704037]
We propose a deep generative model of single-cell gene expression data for which each perturbation is treated as an intervention targeting an unknown, but sparse, subset of latent variables.
We benchmark these methods on simulated single-cell data to evaluate their performance at latent units recovery, causal target identification and out-of-domain generalization.
arXiv Detail & Related papers (2022-11-07T15:47:40Z) - Towards an Automatic Analysis of CHO-K1 Suspension Growth in
Microfluidic Single-cell Cultivation [63.94623495501023]
We propose a novel Machine Learning architecture, which allows us to infuse a neural deep network with human-powered abstraction on the level of data.
Specifically, we train a generative model simultaneously on natural and synthetic data, so that it learns a shared representation, from which a target variable, such as the cell count, can be reliably estimated.
arXiv Detail & Related papers (2020-10-20T08:36:51Z) - A Cross-Level Information Transmission Network for Predicting Phenotype
from New Genotype: Application to Cancer Precision Medicine [37.442717660492384]
We propose a novel Cross-LEvel Information Transmission network (CLEIT) framework.
Inspired by domain adaptation, CLEIT first learns the latent representation of high-level domain then uses it as ground-truth embedding.
We demonstrate the effectiveness and performance boost of CLEIT in predicting anti-cancer drug sensitivity from somatic mutations.
arXiv Detail & Related papers (2020-10-09T22:01:00Z) - A Systematic Approach to Featurization for Cancer Drug Sensitivity
Predictions with Deep Learning [49.86828302591469]
We train >35,000 neural network models, sweeping over common featurization techniques.
We found the RNA-seq to be highly redundant and informative even with subsets larger than 128 features.
arXiv Detail & Related papers (2020-04-30T20:42:17Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.