Evidence map›Paper›PMID 33655208›Full record

ArticleNAR genomics and bioinformatics2021

Single-cell mapper (scMappR): using scRNA-seq to infer the cell-type specificities of differentially expressed genes.

Dustin J Sokolowski, Mariela Faykoo-Martinez, Lauren Erdman, Huayun Hou, Cadia Chan, Helen Zhu, Melissa M Holmes, Anna Goldenberg, Michael D Wilson

Open access · goldAbstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Time series transcriptome analysis implicates the circadian clock in theProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. The genetic source tracking of human urinary exosomes.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  20. Article
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

9 authors at 3 institutions in 1 country.

Dustin J SokolowskiDepartment of Molecular Genetics, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Mariela Faykoo-MartinezGenetics and Genome Biology, SickKids Research Institute, Toronto, ON, M5G 0A4, Canada.
Lauren ErdmanGenetics and Genome Biology, SickKids Research Institute, Toronto, ON, M5G 0A4, Canada.
Huayun HouDepartment of Molecular Genetics, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Cadia ChanDepartment of Molecular Genetics, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Helen ZhuDepartment of Medical Biophysics, University of Toronto, Toronto, ON, M5G 1L7, Canada.
Melissa M HolmesDepartment of Cell and Systems Biology, University of Toronto, Toronto, ON, M5S 3G5, Canada.
Anna GoldenbergGenetics and Genome Biology, SickKids Research Institute, Toronto, ON, M5G 0A4, Canada.
Michael D WilsonDepartment of Molecular Genetics, University of Toronto, Toronto, ON, M5S 1A8, Canada.ORCID https://orcid.org/0000-0002-4015-3066
University of Toronto · CACanadian Institute for Advanced Research · CAUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA sequencing (RNA-seq) is widely used to identify differentially expressed genes (DEGs) and reveal biological mechanisms underlying complex biological processes. RNA-seq is often performed on heterogeneous samples and the resulting DEGs do not necessarily indicate the cell-types where the differential expression occurred. While single-cell RNA-seq (scRNA-seq) methods solve this problem, technical and cost constraints currently limit its widespread use. Here we present single cell Mapper (scMappR), a method that assigns cell-type specificity scores to DEGs obtained from bulk RNA-seq by leveraging cell-type expression data generated by scRNA-seq and existing deconvolution methods. After evaluating scMappR with simulated RNA-seq data and benchmarking scMappR using RNA-seq data obtained from sorted blood cells, we asked if scMappR could reveal known cell-type specific changes that occur during kidney regeneration. scMappR appropriately assigned DEGs to cell-types involved in kidney regeneration, including a relatively small population of immune cells. While scMappR can work with user-supplied scRNA-seq data, we curated scRNA-seq expression matrices for ∼100 human and mouse tissues to facilitate its stand-alone use with bulk RNA-seq data from these species. Overall, scMappR is a user-friendly R package that complements traditional differential gene expression analysis of bulk RNA-seq data.

Identifiers

PMID33655208
PMCPMC7902236
OpenAlexW3129861733

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.