Evidence map›Paper›PMID 32703984›Full record

ArticleScientific reports2020

Identification of cell types from single cell data using stable clustering.

Azam Peyvandipour, Adib Shafi, Nafiseh Saberian, Sorin Draghici

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

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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

23 citing papers in PubMed.

  1. Article
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  8. The impact of dropouts in scRNAseq dense neighborhood analysis.Computational and structural biotechnology journal · 2025
    Article
  9. Article
  10. The specious art of single-cell genomics.PLoS computational biology · 2023
    Article
  11. Article
  12. Article
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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

4 authors.

Azam PeyvandipourDepartment of Computer Science, Wayne State University, Detroit, MI, USA.
Adib ShafiDepartment of Computer Science, Wayne State University, Detroit, MI, USA.
Nafiseh SaberianDepartment of Computer Science, Wayne State University, Detroit, MI, USA.
Sorin DraghiciDepartment of Computer Science, Wayne State University, Detroit, MI, USA. Sorin@wayne.edu.ORCID http://orcid.org/0000-0002-0786-8377

Funding

Serine/threonine Protein Phosphatase 1 in Insulin resistance and Type 2 DiabetesR01DK107666 · NIDDK · WAYNE STATE UNIVERSITY · PI YI, ZHENGPING · 2015 to 2019
$2.6M
NIDDK NIH HHS 1R01DK107666-01
6 · The paper itself

Abstract

Single-cell RNA-seq (scRNASeq) has become a powerful technique for measuring the transcriptome of individual cells. Unlike the bulk measurements that average the gene expressions over the individual cells, gene measurements at individual cells can be used to study several different tissues and organs at different stages. Identifying the cell types present in the sample from the single cell transcriptome data is a common goal in many single-cell experiments. Several methods have been developed to do this. However, correctly identifying the true cell types remains a challenge. We present a framework that addresses this problem. Our hypothesis is that the meaningful characteristics of the data will remain despite small perturbations of data. We validate the performance of the proposed method on eight publicly available scRNA-seq datasets with known cell types as well as five simulation datasets with different degrees of the cluster separability. We compare the proposed method with five other existing methods: RaceID, SNN-Cliq, SINCERA, SEURAT, and SC3. The results show that the proposed method performs better than the existing methods.

Indexed as

AlgorithmsHigh-Throughput Nucleotide SequencingSequence Analysis, RNASingle-Cell AnalysisTranscriptomeCluster AnalysisComputer Simulation

Identifiers

PMID32703984
PMCPMC7378075

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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.