Dimension Reduction and Clustering of Single Cell Calcium Spiking: Comparison of t-SNE and UMAP

Author(s):  
Suman Gare ◽  
Soumita Chel ◽  
Manohar Kuruba ◽  
Soumya Jana ◽  
Lopamudra Giri
2011 ◽  
Vol 31 (6) ◽  
pp. 835-846 ◽  
Author(s):  
R. A. De Melo Reis ◽  
C. S. Schitine ◽  
A. Kofalvi ◽  
S. Grade ◽  
L. Cortes ◽  
...  

2020 ◽  
Vol 21 (1) ◽  
Author(s):  
F. William Townes ◽  
Stephanie C. Hicks ◽  
Martin J. Aryee ◽  
Rafael A. Irizarry

2019 ◽  
Vol 20 (1) ◽  
Author(s):  
F. William Townes ◽  
Stephanie C. Hicks ◽  
Martin J. Aryee ◽  
Rafael A. Irizarry

AbstractSingle-cell RNA-Seq (scRNA-Seq) profiles gene expression of individual cells. Recent scRNA-Seq datasets have incorporated unique molecular identifiers (UMIs). Using negative controls, we show UMI counts follow multinomial sampling with no zero inflation. Current normalization procedures such as log of counts per million and feature selection by highly variable genes produce false variability in dimension reduction. We propose simple multinomial methods, including generalized principal component analysis (GLM-PCA) for non-normal distributions, and feature selection using deviance. These methods outperform the current practice in a downstream clustering assessment using ground truth datasets.


2011 ◽  
Vol 6 (3) ◽  
pp. 288-296 ◽  
Author(s):  
Maria Francisca Eiriz ◽  
Sofia Grade ◽  
Alexandra Rosa ◽  
Sara Xapelli ◽  
Liliana Bernardino ◽  
...  

2017 ◽  
Author(s):  
Dongfang Wang ◽  
Jin Gu

AbstractSingle cell RNA sequencing (scRNA-seq) is a powerful technique to analyze the transcriptomic heterogeneities in single cell level. It is an important step for studying cell sub-populations and lineages based on scRNA-seq data by finding an effective low-dimensional representation and visualization of the original data. The scRNA-seq data are much noiser than traditional bulk RNA-Seq: in the single cell level, the transcriptional fluctuations are much larger than the average of a cell population and the low amount of RNA transcripts will increase the rate of technical dropout events. In this study, we proposed VASC (deep Variational Autoencoder for scRNA-seq data), a deep multi-layer generative model, for the unsupervised dimension reduction and visualization of scRNA-seq data. It can explicitly model the dropout events and find the nonlinear hierarchical feature representations of the original data. Tested on twenty datasets, VASC shows superior performances in most cases and broader dataset compatibility compared with four state-of-the-art dimension reduction methods. Then, for a case study of pre-implantation embryos, VASC successfully re-establishes the cell dynamics and identifies several candidate marker genes associated with the early embryo development.


2019 ◽  
Author(s):  
Svetlana Ovchinnikova ◽  
Simon Anders

AbstractDimension-reduction methods, such as t-SNE or UMAP, are widely used when exploring high-dimensional data describing many entities, e.g., RNA-seq data for many single cells. However, dimension reduction is commonly prone to introducing artefacts, and we hence need means to see where a dimension-reduced embedding is a faithful representation of the local neighbourhood and where it is not.We present Sleepwalk, a simple but powerful tool that allows the user to interactively explore an embedding, using colour to depict original or any other distances from all points to the cell under the mouse cursor. We show how this approach not only highlights distortions, but also reveals otherwise hidden characteristics of the data, and how Sleep-walk’s comparative modes help integrate multi-sample data and understand differences between embedding and preprocessing methods. Sleepwalk is a versatile and intuitive tool that unlocks the full power of dimension reduction and will be of value not only in single-cell RNA-seq but also in any other area with matrix-shaped big data.


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