Trajectory Inference with Cell-Cell Interactions (TICCI): intercellular communication improves the accuracy of trajectory inference methods.

Yifeng Fu, Hong Qu, Dacheng Qu, Min Zhao
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Abstract

Motivation: Understanding cell differentiation and development dynamics is key for single-cell transcriptome analysis. Current cell differentiation trajectory inference algorithms face challenges such as high dimensionality, noise, and a need for users to possess certain biological information about the datasets to effectively utilize the algorithms. Here, we introduce Trajectory Inference with Cell-Cell Interaction (TICCI), a novel way to address these challenges by integrating intercellular communication information. In recognizing crucial intercellular communication during development, TICCI proposes Cell-Cell Interactions (CCI) at single-cell resolution. We posit that cells exhibiting higher gene expression similarity patterns are more likely to exchange information via biomolecular mediators.

Results: TICCI is initiated by constructing a cell-neighborhood matrix using edge weights composed of intercellular similarity and CCI information. Louvain partitioning identifies trajectory branches, attenuating noise, while single-cell entropy (scEntropy) is used to assess differentiation status. The Chu-Liu algorithm constructs a directed least-square model to identify trajectory branches, and an improved diffusion fitted time algorithm computes cell-fitted time in nonconnected topologies. TICCI validation on single-cell RNA sequencing (scRNA-seq) datasets confirms the accuracy of cell trajectories, aligning with genealogical branching and gene markers. Verification using extrinsic information labels demonstrates CCI information utility in enhancing accurate trajectory inference. A comparative analysis establishes TICCI proficiency in accurate temporal ordering.

Availability and implementation: Source code and binaries freely available for download at https://github.com/mine41/TICCI, implemented in R (version 4.32) and Python (version 3.7.16) and supported on MS Windows. Authors ensure that the software is available for a full two years following publication.

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基于细胞间相互作用的轨迹推断(TICCI):细胞间通信提高了轨迹推断方法的准确性。
动机:了解细胞分化和发育动力学是单细胞转录组分析的关键。当前的细胞分化轨迹推断算法面临着诸如高维、噪声以及需要用户拥有有关数据集的某些生物信息才能有效利用算法等挑战。在这里,我们引入了基于细胞-细胞相互作用的轨迹推断(TICCI),这是一种通过整合细胞间通信信息来解决这些挑战的新方法。为了识别发育过程中至关重要的细胞间通讯,TICCI提出了单细胞分辨率的细胞-细胞相互作用(CCI)。我们假设,表现出较高基因表达相似模式的细胞更有可能通过生物分子介质交换信息。结果:利用由细胞间相似性和CCI信息组成的边权构建细胞邻域矩阵,从而启动了TICCI。Louvain划分识别轨迹分支,衰减噪声,而单细胞熵(scEntropy)用于评估分化状态。Chu-Liu算法构建了一个有向最小二乘模型来识别轨迹分支,改进的扩散拟合时间算法计算非连通拓扑中的细胞拟合时间。单细胞RNA测序(scRNA-seq)数据集上的TICCI验证证实了细胞轨迹的准确性,与谱系分支和基因标记一致。外部信息标签的验证证明了CCI信息在提高准确轨迹推断方面的效用。对比分析确立了TICCI在准确时间排序方面的熟练程度。可用性和实现:源代码和二进制文件可在https://github.com/mine41/TICCI免费下载,使用R(版本4.32)和Python(版本3.7.16)实现,并支持MS Windows。作者确保该软件在出版后整整两年内可用。补充信息:补充数据可在生物信息学在线获取。
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