Multimodal learning for mapping genotype-phenotype dynamics.

IF 12 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS
Farhan Khodaee, Rohola Zandie, Elazer R Edelman
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引用次数: 0

Abstract

How complex phenotypes emerge from intricate gene expression patterns is a fundamental question in biology. Integrating high-content genotyping approaches such as single-cell RNA sequencing and advanced learning methods such as language models offers an opportunity for dissecting this complex relationship. Here we present a computational integrated genetics framework designed to analyze and interpret the high-dimensional landscape of genotypes and their associated phenotypes simultaneously. We applied this approach to develop a multimodal foundation model to explore the genotype-phenotype relationship manifold for human transcriptomics at the cellular level. Analyzing this joint manifold showed a refined resolution of cellular heterogeneity, uncovered potential cross-tissue biomarkers and provided contextualized embeddings to investigate the polyfunctionality of genes shown for the von Willebrand factor (VWF) gene in endothelial cells. Overall, this study advances our understanding of the dynamic interplay between gene expression and phenotypic manifestation and demonstrates the potential of integrated genetics in uncovering new dimensions of cellular function and complexity.

绘制基因型-表型动力学的多模态学习。
复杂的表型是如何从复杂的基因表达模式中产生的,这是生物学中的一个基本问题。整合高含量的基因分型方法,如单细胞RNA测序和先进的学习方法,如语言模型,为剖析这种复杂的关系提供了机会。在这里,我们提出了一个计算集成遗传学框架,旨在同时分析和解释基因型及其相关表型的高维景观。我们应用这种方法开发了一个多模态基础模型,在细胞水平上探索人类转录组学的基因型-表型关系。分析这种联合歧管显示了细胞异质性的精细分辨率,揭示了潜在的跨组织生物标志物,并提供了上下文嵌入来研究内皮细胞中血管性血液病因子(VWF)基因的多功能性。总的来说,这项研究促进了我们对基因表达和表型表现之间动态相互作用的理解,并展示了综合遗传学在揭示细胞功能和复杂性的新维度方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
11.70
自引率
0.00%
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