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Biology subjects

Gao, Y.-L.

Publications and source records attributed to Gao, Y.-L..

3 recordsLinked to original sources

Bringing the Genetically Minimal Cell to Life on a Computer in 4D

We present a whole-cell spatial and kinetic model for the 100 minute cell cycle of the genetically minimal bacterium, JCVI-syn3A. This is the first simulation of a complete cell cycle in 4D including all genetic information processes, metabolic networks, growth, and cell division. Integrating hybrid computational methods, dynamics of the morphological transformations were achieved. Growth is driven by synthesis of lipids and membrane proteins and constrained by new fluorescence imaging data. Chromosome replication and segregation is controlled by essential SMC and topoisomerase proteins in Brownian dynamics simulations with replication rates responding to dNTP pools from metabolism. The model captures the origin to terminus ratio measured in our DNA sequencing and recovers other experimental measurements like doubling time, mRNA half-lives, protein distributions, and ribosome counts. Because of stochasticity, each replicate cell is unique. Not only do we predict average behavior for partitioning to daughter cells, we predict the heterogeneity among them.

biophysics↗

Characterization of epigenetic alterations in esophageal cancer by whole-genome bisulfite sequencing

Esophageal carcinoma is a common and aggressive malignancy, and its patients have dismal clinical outcomes. The epigenetic dysregulation in both major subtypes, esophageal squamous cell carcinoma (ESCC) and adenocarcinoma (EAC), awaits further characterization. Here, we perform whole-genome bisulfite sequencing (WGBS) on a total of 43 esophageal cancer and normal samples, generating one of the largest WGBS datasets in this cancer to date. Focusing on hypomethylated regions in cancer, we show that they are associated with increased chromatin activity and enhancer RNA expression. Using this large collection of WGBS dataset, we reveal and validate novel clusters in both ESCC and EAC. We further identify specific molecular features in each cluster, with potential clinical implications. These data together advance our understanding of the epigenetic alterations in esophageal cancer and provide a rich resource for the research community of this disease.

cancer biology↗

CNLLRR: A Novel Low-Rank Representation Method for Single-cell RNA-seq Data Analysis

The development of single-cell RNA-sequencing (scRNA-seq) technology has enabled the measurement of gene expression in individual cells. This provides an unprecedented opportunity to explore the biological mechanisms at the cellular level. However, existing scRNA-seq analysis methods are susceptible to noise and outliers or ignore the manifold structure inherent in the data. In this paper, a novel method called Cauchy non-negative Laplacian regularized low-rank representation (CNLLRR) is proposed to alleviate the above problem. Specifically, we employ the Cauchy loss function (CLF) instead of the conventional norm constraints in the noise matrix of CNLLRR, which will enhance the robustness of the method. In addition, graph regularization term is applied to the objective function, which can capture the paired geometric relationships between cells. Then, alternating direction method of multipliers (ADMM) is adopted to solve the optimization problem of CNLLRR. Finally, extensive experiments on scRNA-seq data reveal that the proposed CNLLRR method outperforms other state-of-the-art methods for cell clustering, cell visualization and prioritization of gene markers. CNLLRR contributes to understand the heterogeneity between cell populations in complex biological systems.\n\nAuthor summaryAnalysis of single-cell data can help to further study the heterogeneity and complexity of cell populations. The current analysis methods are mainly to learn the similarity between cells and cells. Then they use the clustering algorithm to perform cell clustering or downstream analysis on the obtained similarity matrix. Therefore, constructing accurate cell-to-cell similarity is crucial for single-cell data analysis. In this paper, we design a novel Cauchy non-negative Laplacian regularized low-rank representation (CNLLRR) method to get a better similarity matrix. Specifically, Cauchy loss function (CLF) constraint is applied to punish noise matrix, which will improve the robustness of CNLLRR to noise and outliers. Moreover, graph regularization term is applied to the objective function, which will effectively encode the local manifold information of the data. Further, these will guarantee the quality of the cell-to-cell similarity matrix learned. Finally, single-cell data analysis experiments show that our method is superior to other representative methods.

bioinformatics↗