Discovering Governing Equations of Biological Systems through Representation Learning and Sparse Model Discovery
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Abstract
Understanding the governing rules of complex biological systems remains a significant challenge due to the nonlinear, high-dimensional nature of biological data. In this study, we present CLERA, a novel end-to-end computational framework designed to uncover parsimonious dynamical models and identify active gene programs from single-cell RNA sequencing data. By integrating a supervised autoencoder architecture with Sparse Identification of Nonlinear Dynamics, CLERA leverages prior knowledge to simultaneously extract related low-dimensional embeddings and uncovers the underlying dynamical systems that drive the processes. Through the analysis of both synthetic and biological datasets, CLERA demonstrates robust performance in reconstructing gene expression dynamics, identifying key regulatory genes, and capturing temporal patterns across distinct cell types. CLERA’s ability to generate dynamic interaction networks, combined with network rewiring using Personalized PageRank to highlight central genes and active gene programs, offers new insights into the complex regulatory mechanisms underlying cellular processes.
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- Deep Lineage: Single-Cell Lineage Tracing and Fate Inference Using Deep Learning via crossref
- The Power of Two: integrating deep diffusion models and variational autoencoders for single-cell transcriptomics analysis via crossref
- doi:10.1038/s41598-022-06159-x via crossref
- doi:10.1016/j.physrep.2023.10.005 via crossref
- doi:10.1038/s41598-022-13644-w via crossref
- doi:10.1073/pnas.1517384113 via crossref
- doi:10.1093/bioadv/vbad166 via crossref
- doi:10.1093/nar/gku555 via crossref
- doi:10.1038/s41576-019-0142-2 via crossref
- doi:10.7554/elife.81464 via crossref
- doi:10.1007/s11071-021-07118-3 via crossref
- doi:10.1145/3501714.3501755 via crossref
- doi:10.1016/j.patter.2023.100844 via crossref
- doi:10.1038/s41592-019-0494-8 via crossref
- doi:10.1016/j.crmeth.2024.100819 via crossref
- doi:10.1038/s41467-018-07931-2 via crossref
- doi:10.1242/dev.201280 via crossref
- doi:10.1016/j.cels.2020.08.003 via crossref
- doi:10.1145/775152.775191 via crossref
- doi:10.1242/dev.173849 via crossref
- doi:10.1210/endocr/bqaa233 via crossref
- doi:10.3389/fcell.2021.629212 via crossref
- doi:10.1002/dvdy.20729 via crossref
- doi:10.1016/j.pan.2018.09.006 via crossref
- doi:10.1186/s13287-017-0694-z via crossref
- doi:10.1073/pnas.97.4.1607 via crossref
- doi:10.1007/s00125-005-0106-2 via crossref
- doi:10.1038/s41467-023-44384-8 via crossref
- doi:10.1038/s41587-019-0068-4 via crossref
- doi:10.1016/j.exphem.2003.12.007 via crossref
- doi:10.1161/circulationaha.117.029015 via crossref
- doi:10.1038/360741a0 via crossref
- doi:10.1038/s43587-023-00558-z via crossref
- doi:10.1371/journal.pbio.3001121 via crossref
- doi:10.1109/cvpr46437.2021.00947 via crossref
- doi:10.1038/323533a0 via crossref
- doi:10.1371/journal.pcbi.1008235 via crossref
- doi:10.1016/j.isci.2021.102245 via crossref
- doi:10.1186/s12964-021-00706-1 via crossref
- doi:10.1073/pnas.1906995116 via crossref
- doi:10.1080/00273171.2019.1566050 via crossref
- doi:10.1186/s12885-022-09211-1 via crossref
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