Evidence map›Paper›PMID 30774736›Full record

ArticleStatistics in biosciences2017

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

Courtney Schiffman, Christina Lin, Funan Shi, Luonan Chen, Lydia Sohn, Haiyan Huang

Abstract read
In one paragraph

Article in Statistics in biosciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Shared Differential Expression-Based Distance Reflects Global Cell Type Relationships in Single-Cell RNA Sequencing Data.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  3. Network Modeling in Biology: Statistical Methods for Gene and Brain Networks.Statistical science : a review journal of the Institute of Mathematical Statistics · 2021
    Article
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Courtney SchiffmanDepartment of Biostatistics, UC Berkeley, Berkeley, USA.
Christina LinDepartment of Chemical Biology and Department of Molecular and Cellular Biology, UC Berkeley, Berkeley, USA.
Funan ShiDepartment of Statistics, UC Berkeley, Berkeley, USA.
Luonan ChenKey Laboratory of Systems Biology, Innovation Center for Cell Signaling Network, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Lydia SohnDepartment of Mechanical Engineering, UC Berkeley, Berkeley, USA.
Haiyan HuangDepartment of Statistics, UC Berkeley, Berkeley, USA.

Funding

Removing statistical bottle-necks in data analysis for the ENCODE ConsortiumU01HG007031 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI BICKEL, PETER J · 2012 to 2015
$1.5M
Isolating Circulating Tumor CellsR21CA182375 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI SOHN, LYDIA L · 2015 to 2017
$605k
NCI NIH HHS R21 CA182375NHGRI NIH HHS U01 HG007031
6 · The paper itself

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.

Indexed as

EMT inducers (Thrombin, TGFB-1)ovarian cancersimilarity measuresingle-cell clusteringsingle-cell RNA sequencing (scRNA seq)subpopulation identification

Identifiers

PMID30774736
PMCPMC6377168

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.