Graph Structure Learning for Tumor Microenvironment with Cell Type Annotation from non-spatial scRNA-seq data
- URL: http://arxiv.org/abs/2502.02629v1
- Date: Tue, 04 Feb 2025 18:28:25 GMT
- Title: Graph Structure Learning for Tumor Microenvironment with Cell Type Annotation from non-spatial scRNA-seq data
- Authors: Yu-An Huang, Yue-Chao Li, Hai-Ru You, Jie Pan, Xiyue Cao, Xinyuan Li, Zhi-An Huang, Zhu-Hong You,
- Abstract summary: We present a novel graph neural network (GNN) model that enhances cell type prediction and cell interaction analysis.
The proposed scGSL model demonstrated robust performance, achieving an average accuracy of 84.83%, precision of 86.23%, recall of 81.51%, and an F1 score of 80.92% across all datasets.
- Score: 6.432270457083369
- License:
- Abstract: The exploration of cellular heterogeneity within the tumor microenvironment (TME) via single-cell RNA sequencing (scRNA-seq) is essential for understanding cancer progression and response to therapy. Current scRNA-seq approaches, however, lack spatial context and rely on incomplete datasets of ligand-receptor interactions (LRIs), limiting accurate cell type annotation and cell-cell communication (CCC) inference. This study addresses these challenges using a novel graph neural network (GNN) model that enhances cell type prediction and cell interaction analysis. Our study utilized a dataset consisting of 49,020 cells from 19 patients across three cancer types: Leukemia, Breast Invasive Carcinoma, and Colorectal Cancer. The proposed scGSL model demonstrated robust performance, achieving an average accuracy of 84.83%, precision of 86.23%, recall of 81.51%, and an F1 score of 80.92% across all datasets. These metrics represent a significant enhancement over existing methods, which typically exhibit lower performance metrics. Additionally, by reviewing existing literature on gene interactions within the TME, the scGSL model proves to robustly identify biologically meaningful gene interactions in an unsupervised manner, validated by significant expression differences in key gene pairs across various cancers. The source code and data used in this paper can be found in https://github.com/LiYuechao1998/scGSL.
Related papers
- scBIT: Integrating Single-cell Transcriptomic Data into fMRI-based Prediction for Alzheimer's Disease Diagnosis [24.268703526039367]
scBIT is a novel method for enhancing Alzheimer's disease (AD) prediction by combining fMRI with single-nucleus RNA (snRNA)
It employs a sampling strategy to segment snRNA data into cell-type-specific gene networks and utilizes a self-explainable graph neural network to extract critical subgraphs.
Extensive experiments validate scBIT's effectiveness in revealing intricate brain region-gene associations.
arXiv Detail & Related papers (2025-02-04T18:37:46Z) - Pan-cancer gene set discovery via scRNA-seq for optimal deep learning based downstream tasks [6.869831177092736]
We analyzed scRNA-seq data from 181 tumor biopsies across 13 cancer types.
High-dimensional weighted gene co-expression network analysis (hdWGCNA) was performed to identify relevant gene sets.
Oncogenes from OncoKB evaluated with deep learning models, including multilayer perceptrons (MLPs) and graph neural networks (GNNs)
arXiv Detail & Related papers (2024-08-13T23:24:36Z) - scBiGNN: Bilevel Graph Representation Learning for Cell Type
Classification from Single-cell RNA Sequencing Data [62.87454293046843]
Graph neural networks (GNNs) have been widely used for automatic cell type classification.
scBiGNN comprises two GNN modules to identify cell types.
scBiGNN outperforms a variety of existing methods for cell type classification from scRNA-seq data.
arXiv Detail & Related papers (2023-12-16T03:54:26Z) - 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) - Breast Cancer Histopathology Image based Gene Expression Prediction
using Spatial Transcriptomics data and Deep Learning [3.583756449759971]
We present BrST-Net, a deep learning framework for predicting gene expression from histopathology images.
We trained and evaluated 10 state-of-the-art deep learning models without utilizing pretrained weights for the prediction of 250 genes.
Our methodology outperforms previous studies, with 237 genes identified with positive correlation, including 24 genes with a median correlation coefficient greater than 0.50.
arXiv Detail & Related papers (2023-03-17T14:03:40Z) - Machine Learning Methods for Cancer Classification Using Gene Expression
Data: A Review [77.34726150561087]
Cancer is the second major cause of death after cardiovascular diseases.
Gene expression can play a fundamental role in the early detection of cancer.
This study reviews recent progress in gene expression analysis for cancer classification using machine learning methods.
arXiv Detail & Related papers (2023-01-28T15:03:03Z) - Multiple Instance Neural Networks Based on Sparse Attention for Cancer
Detection using T-cell Receptor Sequences [10.199698726118003]
We propose multiple instance neural networks based on sparse attention (MINN-SA) to enhance the performance in cancer detection and explainability.
MINN-SA yields the highest area under the ROC curve (AUC) scores on average measured across 10 different types of cancers.
arXiv Detail & Related papers (2022-08-09T03:24:03Z) - Predicting Molecular Phenotypes with Single Cell RNA Sequencing Data: an
Assessment of Unsupervised Machine Learning Models [0.0]
This study is to evaluate unsupervised machine learning on classifying treatment-resistant phenotypes in heterogeneous tumors.
scRNAseq quantifies mRNA in cells and characterizes cell phenotypes.
clusters generated from this pipeline can be used to understand cancer cell behavior and malignant growth.
arXiv Detail & Related papers (2021-08-11T05:30:37Z) - Cancer Gene Profiling through Unsupervised Discovery [49.28556294619424]
We introduce a novel, automatic and unsupervised framework to discover low-dimensional gene biomarkers.
Our method is based on the LP-Stability algorithm, a high dimensional center-based unsupervised clustering algorithm.
Our signature reports promising results on distinguishing immune inflammatory and immune desert tumors.
arXiv Detail & Related papers (2021-02-11T09:04:45Z) - Topological Data Analysis of copy number alterations in cancer [70.85487611525896]
We explore the potential to capture information contained in cancer genomic information using a novel topology-based approach.
We find that this technique has the potential to extract meaningful low-dimensional representations in cancer somatic genetic data.
arXiv Detail & Related papers (2020-11-22T17:31:23Z) - 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.