G2{\Phi}net: Relating Genotype and Biomechanical Phenotype of Tissues
with Deep Learning
- URL: http://arxiv.org/abs/2208.09889v1
- Date: Sun, 21 Aug 2022 14:22:37 GMT
- Title: G2{\Phi}net: Relating Genotype and Biomechanical Phenotype of Tissues
with Deep Learning
- Authors: Enrui Zhang, Bart Spronck, Jay D. Humphrey, George Em Karniadakis
- Abstract summary: We present a novel genotype-to-biomechanical-phenotype neural network (G2Phinet) for characterizing and classifying biomechanical properties of soft tissues.
G2Phinet can infer the biomechanical response while simultaneously ascribing the associated genotype correctly.
- Score: 0.18352113484137625
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Many genetic mutations adversely affect the structure and function of
load-bearing soft tissues, with clinical sequelae often responsible for
disability or death. Parallel advances in genetics and histomechanical
characterization provide significant insight into these conditions, but there
remains a pressing need to integrate such information. We present a novel
genotype-to-biomechanical-phenotype neural network (G2{\Phi}net) for
characterizing and classifying biomechanical properties of soft tissues, which
serve as important functional readouts of tissue health or disease. We
illustrate the utility of our approach by inferring the nonlinear,
genotype-dependent constitutive behavior of the aorta for four mouse models
involving defects or deficiencies in extracellular constituents. We show that
G2{\Phi}net can infer the biomechanical response while simultaneously ascribing
the associated genotype correctly by utilizing limited, noisy, and unstructured
experimental data. More broadly, G2{\Phi}net provides a powerful method and a
paradigm shift for correlating genotype and biomechanical phenotype
quantitatively, promising a better understanding of their interplay in
biological tissues.
Related papers
- AI-driven multi-omics integration for multi-scale predictive modeling of causal genotype-environment-phenotype relationships [9.909750609459074]
We propose a new artificial intelligence (AI)-powered biology-inspired multi-scale modeling framework to tackle these issues.
This framework will integrate multi-omics data across biological levels, organism hierarchies, and species to predict causal genotype-environment-phenotype relationships under various conditions.
arXiv Detail & Related papers (2024-07-08T21:23:25Z) - 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) - Causal machine learning for single-cell genomics [94.28105176231739]
We discuss the application of machine learning techniques to single-cell genomics and their challenges.
We first present the model that underlies most of current causal approaches to single-cell biology.
We then identify open problems in the application of causal approaches to single-cell data.
arXiv Detail & Related papers (2023-10-23T13:35:24Z) - 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) - Genetic prediction of quantitative traits: a machine learner's guide
focused on height [0.0]
We provide an overview for the machine learning community on current state of the art models and associated subtleties.
We use height as an example of a continuous-valued phenotype and provide an introduction to benchmark datasets, confounders, feature selection, and common metrics.
arXiv Detail & Related papers (2023-10-06T05:43:50Z) - Knowledge Graph Completion based on Tensor Decomposition for Disease
Gene Prediction [2.838553480267889]
We construct a biological knowledge graph centered on diseases and genes, and develop an end-to-end Knowledge graph completion model for Disease Gene Prediction.
KDGene introduces an interaction module between the embeddings of entities and relations to tensor decomposition, which can effectively enhance the information interaction in biological knowledge.
arXiv Detail & Related papers (2023-02-18T13:57:44Z) - 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) - SemanticCAP: Chromatin Accessibility Prediction Enhanced by Features
Learning from a Language Model [3.0643865202019698]
We propose a new solution named SemanticCAP to identify accessible regions of the genome.
It introduces a gene language model which models the context of gene sequences, thus being able to provide an effective representation of gene sequences.
Compared with other systems under public benchmarks, our model proved to have better performance.
arXiv Detail & Related papers (2022-04-05T11:47:58Z) - Factored Attention and Embedding for Unstructured-view Topic-related
Ultrasound Report Generation [70.7778938191405]
We propose a novel factored attention and embedding model (termed FAE-Gen) for the unstructured-view topic-related ultrasound report generation.
The proposed FAE-Gen mainly consists of two modules, i.e., view-guided factored attention and topic-oriented factored embedding, which capture the homogeneous and heterogeneous morphological characteristic across different views.
arXiv Detail & Related papers (2022-03-12T15:24:03Z) - 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) - 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)
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.