Literature DB >> 30774736

SIDEseq: A Cell Similarity Measure Defined by Shared Identified Differentially Expressed Genes for Single-Cell RNA sequencing Data.

Courtney Schiffman1, Christina Lin2, Funan Shi3, Luonan Chen4, Lydia Sohn5, Haiyan Huang3.   

Abstract

One goal of single-cell RNA sequencing (scRNA seq) is to expose possible heterogeneity within cell populations due to meaningful, biological variation. Examining cell-to-cell heterogeneity, and further, identifying subpopulations of cells based on scRNA seq data has been of common interest in life science research. A key component to successfully identifying cell subpopulations (or clustering cells) is the (dis)similarity measure used to group the cells. In this paper, we introduce a novel measure, named SIDEseq, to assess cell-to-cell similarity using scRNA seq data. SIDEseq first identifies a list of putative differentially expressed (DE) genes for each pair of cells. SIDEseq then integrates the information from all the DE gene lists (corresponding to all pairs of cells) to build a similarity measure between two cells. SIDEseq can be implemented in any clustering algorithm that requires a (dis)similarity matrix. This new measure incorporates information from all cells when evaluating the similarity between any two cells, a characteristic not commonly found in existing (dis)similarity measures. This property is advantageous for two reasons: (a) borrowing information from cells of different subpopulations allows for the investigation of pairwise cell relationships from a global perspective and (b) information from other cells of the same subpopulation could help to ensure a robust relationship assessment. We applied SIDEseq to a newly generated human ovarian cancer scRNA seq dataset, a public human embryo scRNA seq dataset, and several simulated datasets. The clustering results suggest that the SIDEseq measure is capable of uncovering important relationships between cells, and outperforms or at least does as well as several popular (dis)similarity measures when used on these datasets.

Entities:  

Keywords:  EMT inducers (Thrombin, TGFB-1); ovarian cancer; similarity measure; single-cell RNA sequencing (scRNA seq); single-cell clustering; subpopulation identification

Year:  2017        PMID: 30774736      PMCID: PMC6377168          DOI: 10.1007/s12561-017-9194-z

Source DB:  PubMed          Journal:  Stat Biosci        ISSN: 1867-1764


  30 in total

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Journal:  J Endocrinol       Date:  2006-12       Impact factor: 4.286

2.  Transformation of epithelial ovarian cancer stemlike cells into mesenchymal lineage via EMT results in cellular heterogeneity and supports tumor engraftment.

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3.  Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses.

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Journal:  Nat Protoc       Date:  2012-02-16       Impact factor: 13.491

4.  Suppression versus induction of androgen receptor functions by the phosphatidylinositol 3-kinase/Akt pathway in prostate cancer LNCaP cells with different passage numbers.

Authors:  Hui-Kuan Lin; Yueh-Chiang Hu; Lin Yang; Saleh Altuwaijri; Yen-Ta Chen; Hong-Yo Kang; Chawnshang Chang
Journal:  J Biol Chem       Date:  2003-10-10       Impact factor: 5.157

5.  Evaluation of statistical methods for normalization and differential expression in mRNA-Seq experiments.

Authors:  James H Bullard; Elizabeth Purdom; Kasper D Hansen; Sandrine Dudoit
Journal:  BMC Bioinformatics       Date:  2010-02-18       Impact factor: 3.169

6.  The epithelial-mesenchymal transition generates cells with properties of stem cells.

Authors:  Sendurai A Mani; Wenjun Guo; Mai-Jing Liao; Elinor Ng Eaton; Ayyakkannu Ayyanan; Alicia Y Zhou; Mary Brooks; Ferenc Reinhard; Cheng Cheng Zhang; Michail Shipitsin; Lauren L Campbell; Kornelia Polyak; Cathrin Brisken; Jing Yang; Robert A Weinberg
Journal:  Cell       Date:  2008-05-16       Impact factor: 41.582

7.  Expression of stem cell and epithelial-mesenchymal transition markers in primary breast cancer patients with circulating tumor cells.

Authors:  Sabine Kasimir-Bauer; Oliver Hoffmann; Diethelm Wallwiener; Rainer Kimmig; Tanja Fehm
Journal:  Breast Cancer Res       Date:  2012-01-20       Impact factor: 6.466

8.  Circulating tumour cells escape from EpCAM-based detection due to epithelial-to-mesenchymal transition.

Authors:  Tobias M Gorges; Ingeborg Tinhofer; Michael Drosch; Lars Röse; Thomas M Zollner; Thomas Krahn; Oliver von Ahsen
Journal:  BMC Cancer       Date:  2012-05-16       Impact factor: 4.430

9.  Removing technical variability in RNA-seq data using conditional quantile normalization.

Authors:  Kasper D Hansen; Rafael A Irizarry; Zhijin Wu
Journal:  Biostatistics       Date:  2012-01-27       Impact factor: 5.899

10.  Differential expression analysis for sequence count data.

Authors:  Simon Anders; Wolfgang Huber
Journal:  Genome Biol       Date:  2010-10-27       Impact factor: 13.583

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  4 in total

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2.  Shared Differential Expression-Based Distance Reflects Global Cell Type Relationships in Single-Cell RNA Sequencing Data.

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Review 4.  Towards a Systems Immunology Approach to Unravel Responses to Cancer Immunotherapy.

Authors:  Laura Bracci; Alessandra Fragale; Lucia Gabriele; Federica Moschella
Journal:  Front Immunol       Date:  2020-10-22       Impact factor: 7.561

  4 in total

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