Path-GPTOmic: A Balanced Multi-modal Learning Framework for Survival Outcome Prediction
- URL: http://arxiv.org/abs/2403.11375v1
- Date: Mon, 18 Mar 2024 00:02:48 GMT
- Title: Path-GPTOmic: A Balanced Multi-modal Learning Framework for Survival Outcome Prediction
- Authors: Hongxiao Wang, Yang Yang, Zhuo Zhao, Pengfei Gu, Nishchal Sapkota, Danny Z. Chen,
- Abstract summary: We introduce a new multi-modal Path-GPTOmic" framework for cancer survival outcome prediction.
We regulate the embedding space of a foundation model, scGPT, initially trained on single-cell RNA-seq data.
We propose a gradient modulation mechanism tailored to the Cox partial likelihood loss for survival prediction.
- Score: 14.204637932937082
- License: http://creativecommons.org/licenses/by-sa/4.0/
- Abstract: For predicting cancer survival outcomes, standard approaches in clinical research are often based on two main modalities: pathology images for observing cell morphology features, and genomic (e.g., bulk RNA-seq) for quantifying gene expressions. However, existing pathology-genomic multi-modal algorithms face significant challenges: (1) Valuable biological insights regarding genes and gene-gene interactions are frequently overlooked; (2) one modality often dominates the optimization process, causing inadequate training for the other modality. In this paper, we introduce a new multi-modal ``Path-GPTOmic" framework for cancer survival outcome prediction. First, to extract valuable biological insights, we regulate the embedding space of a foundation model, scGPT, initially trained on single-cell RNA-seq data, making it adaptable for bulk RNA-seq data. Second, to address the imbalance-between-modalities problem, we propose a gradient modulation mechanism tailored to the Cox partial likelihood loss for survival prediction. The contributions of the modalities are dynamically monitored and adjusted during the training process, encouraging that both modalities are sufficiently trained. Evaluated on two TCGA(The Cancer Genome Atlas) datasets, our model achieves substantially improved survival prediction accuracy.
Related papers
- 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) - Predicting Genetic Mutation from Whole Slide Images via Biomedical-Linguistic Knowledge Enhanced Multi-label Classification [119.13058298388101]
We develop a Biological-knowledge enhanced PathGenomic multi-label Transformer to improve genetic mutation prediction performances.
BPGT first establishes a novel gene encoder that constructs gene priors by two carefully designed modules.
BPGT then designs a label decoder that finally performs genetic mutation prediction by two tailored modules.
arXiv Detail & Related papers (2024-06-05T06:42:27Z) - Histo-Genomic Knowledge Distillation For Cancer Prognosis From Histopathology Whole Slide Images [7.5123289730388825]
Genome-informed Hyper-Attention Network (G-HANet) is capable of effectively distilling histo-genomic knowledge during training.
Network comprises cross-modal associating branch (CAB) and hyper-attention survival branch (HSB)
arXiv Detail & Related papers (2024-03-15T06:20:09Z) - Pathology-and-genomics Multimodal Transformer for Survival Outcome
Prediction [43.1748594898772]
We propose a multimodal transformer (PathOmics) integrating pathology and genomics insights into colon-related cancer survival prediction.
We emphasize the unsupervised pretraining to capture the intrinsic interaction between tissue microenvironments in gigapixel whole slide images.
We evaluate our approach on both TCGA colon and rectum cancer cohorts, showing that the proposed approach is competitive and outperforms state-of-the-art studies.
arXiv Detail & Related papers (2023-07-22T00:59:26Z) - 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) - Deep Biological Pathway Informed Pathology-Genomic Multimodal Survival
Prediction [7.133948707208067]
We propose PONET- a novel biological pathway-informed pathology-genomic deep model.
Our proposed method achieves superior predictive performance and reveals meaningful biological interpretations.
arXiv Detail & Related papers (2023-01-06T05:24:41Z) - Benchmarking Machine Learning Robustness in Covid-19 Genome Sequence
Classification [109.81283748940696]
We introduce several ways to perturb SARS-CoV-2 genome sequences to mimic the error profiles of common sequencing platforms such as Illumina and PacBio.
We show that some simulation-based approaches are more robust (and accurate) than others for specific embedding methods to certain adversarial attacks to the input sequences.
arXiv Detail & Related papers (2022-07-18T19:16:56Z) - A robust and lightweight deep attention multiple instance learning
algorithm for predicting genetic alterations [4.674211520843232]
We propose a novel Attention-based Multiple Instance Mutation Learning (AMIML) model for predicting gene mutations.
AMIML was comprised of successive 1-D convolutional layers, a decoder, and a residual weight connection to facilitate further integration of a lightweight attention mechanism.
AMIML demonstrated excellent robustness, not only outperforming all the five baseline algorithms in the vast majority of the tested genes, but also providing near-best-performance for the other seven genes.
arXiv Detail & Related papers (2022-05-31T15:45:29Z) - SNP2Vec: Scalable Self-Supervised Pre-Training for Genome-Wide
Association Study [48.75445626157713]
SNP2Vec is a scalable self-supervised pre-training approach for understanding SNP.
We apply SNP2Vec to perform long-sequence genomics modeling.
We evaluate the effectiveness of our approach on predicting Alzheimer's disease risk in a Chinese cohort.
arXiv Detail & Related papers (2022-04-14T01:53:58Z) - Multi-modal Self-supervised Pre-training for Regulatory Genome Across
Cell Types [75.65676405302105]
We propose a simple yet effective approach for pre-training genome data in a multi-modal and self-supervised manner, which we call GeneBERT.
We pre-train our model on the ATAC-seq dataset with 17 million genome sequences.
arXiv Detail & Related papers (2021-10-11T12:48:44Z) - Select-ProtoNet: Learning to Select for Few-Shot Disease Subtype
Prediction [55.94378672172967]
We focus on few-shot disease subtype prediction problem, identifying subgroups of similar patients.
We introduce meta learning techniques to develop a new model, which can extract the common experience or knowledge from interrelated clinical tasks.
Our new model is built upon a carefully designed meta-learner, called Prototypical Network, that is a simple yet effective meta learning machine for few-shot image classification.
arXiv Detail & Related papers (2020-09-02T02:50:30Z)
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.