scholarly journals Machine Learning of Stem Cell Identities From Single-Cell Expression Data via Regulatory Network Archetypes

2019 ◽  
Vol 10 ◽  
Author(s):  
Patrick S. Stumpf ◽  
Ben D. MacArthur
2017 ◽  
Author(s):  
Patrick S Stumpf ◽  
Ben D MacArthur

AbstractThe molecular regulatory network underlying stem cell pluripotency has been intensively studied, and we now have a reliable ensemble model for the ‘average’ pluripotent cell. However, evidence of significant cell-to-cell variability suggests that the activity of this network varies within individual stem cells, leading to differential processing of environmental signals and variability in cell fates. Here, we adapt a method originally designed for face recognition to infer regulatory network patterns within individual cells from single-cell expression data. Using this method we identify three distinct network configurations in cultured mouse embryonic stem cells – corresponding to naïve and formative pluripotent states and an early primitive endoderm state – and associate these configurations with particular combinations of regulatory network activity archetypes that govern different aspects of the cell’s response to environmental stimuli, cell cycle status and core information processing circuitry. These results show how variability in cell identities arise naturally from alterations in underlying regulatory network dynamics and demonstrate how methods from machine learning may be used to better understand single cell biology, and the collective dynamics of cell communities.


2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Aashi Jindal ◽  
Prashant Gupta ◽  
Jayadeva ◽  
Debarka Sengupta

2018 ◽  
Vol 47 (D1) ◽  
pp. D711-D715 ◽  
Author(s):  
Awais Athar ◽  
Anja Füllgrabe ◽  
Nancy George ◽  
Haider Iqbal ◽  
Laura Huerta ◽  
...  

Cell Systems ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 640-652.e5 ◽  
Author(s):  
Fumio Arai ◽  
Patrick S. Stumpf ◽  
Yoshiko M. Ikushima ◽  
Kentaro Hosokawa ◽  
Aline Roch ◽  
...  

Author(s):  
Dongshunyi Li ◽  
Jun Ding ◽  
Ziv Bar-Joseph

Abstract Motivation Recent technological advances enable the profiling of spatial single-cell expression data. Such data present a unique opportunity to study cell–cell interactions and the signaling genes that mediate them. However, most current methods for the analysis of these data focus on unsupervised descriptive modeling, making it hard to identify key signaling genes and quantitatively assess their impact. Results We developed a Mixture of Experts for Spatial Signaling genes Identification (MESSI) method to identify active signaling genes within and between cells. The mixture of experts strategy enables MESSI to subdivide cells into subtypes. MESSI relies on multi-task learning using information from neighboring cells to improve the prediction of response genes within a cell. Applying the methods to three spatial single-cell expression datasets, we show that MESSI accurately predicts the levels of response genes, improving upon prior methods and provides useful biological insights about key signaling genes and subtypes of excitatory neuron cells. Availability and implementation MESSI is available at: https://github.com/doraadong/MESSI


2019 ◽  
Vol 14 (3) ◽  
pp. 255-268 ◽  
Author(s):  
Wei Zhang ◽  
Wenchao Li ◽  
Jianming Zhang ◽  
Ning Wang

Background: Gene Regulatory Network (GRN) inference algorithms aim to explore casual interactions between genes and transcriptional factors. High-throughput transcriptomics data including DNA microarray and single cell expression data contain complementary information in network inference. Objective: To enhance GRN inference, data integration across various types of expression data becomes an economic and efficient solution. Method: In this paper, a novel E-alpha integration rule-based ensemble inference algorithm is proposed to merge complementary information from microarray and single cell expression data. This paper implements a Gradient Boosting Tree (GBT) inference algorithm to compute importance scores for candidate gene-gene pairs. The proposed E-alpha rule quantitatively evaluates the credibility levels of each information source and determines the final ranked list. Results: Two groups of in silico gene networks are applied to illustrate the effectiveness of the proposed E-alpha integration. Experimental outcomes with size50 and size100 in silico gene networks suggest that the proposed E-alpha rule significantly improves performance metrics compared with single information source. Conclusion: In GRN inference, the integration of hybrid expression data using E-alpha rule provides a feasible and efficient way to enhance performance metrics than solely increasing sample sizes.


2018 ◽  
Vol 11 (1) ◽  
Author(s):  
Fatemeh Behjati Ardakani ◽  
Kathrin Kattler ◽  
Karl Nordström ◽  
Nina Gasparoni ◽  
Gilles Gasparoni ◽  
...  

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