Evidence map›Paper›PMID 39404416›Full record

ArticleCells2024

Systematic Comparison of CRISPR and shRNA Screens to Identify Essential Genes Using a Graph-Based Unsupervised Learning Model.

Yulian Ding, Connor Denomy, Andrew Freywald, Yi Pan, Franco J Vizeacoumar, Frederick S Vizeacoumar, Fang-Xiang Wu

Abstract readComparative Study
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Yulian DingCentral for High-Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.ORCID 0000-0001-7435-7094
Connor DenomyDivision of Oncology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0003-1991-5385
Andrew FreywaldDepartment of Pathology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Yi PanCentral for High-Performance Computing, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.ORCID 0000-0002-2766-3096
Franco J VizeacoumarCancer Research Department, Saskatchewan Cancer Agency, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0002-6452-5207
Frederick S VizeacoumarDepartment of Pathology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0002-4676-2911
Fang-Xiang WuDivision of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada.ORCID 0000-0002-4593-9332

Funding

Natural Sciences and Engineering Research Council of Canada (NSERC), RGPIN-2021-03297
6 · The paper itself

Abstract

Generally, essential genes identified using shRNA and CRISPR are not always the same, raising questions about the choice between these two screening platforms. To address this, we systematically compared the performance of CRISPR and shRNA to identify essential genes across different gene expression levels in 254 cell lines. As both platforms have a notable false positive rate, to correct this confounding factor, we first developed a graph-based unsupervised machine learning model to predict common essential genes. Furthermore, to maintain the unique characteristics of individual cell lines, we intersect essential genes derived from the biological experiment with the predicted common essential genes. Finally, we employed statistical methods to compare the ability of these two screening platforms to identify essential genes that exhibit differential expression across various cell lines. Our analysis yielded several noteworthy findings: (1) shRNA outperforms CRISPR in the identification of lowly expressed essential genes; (2) both screening methodologies demonstrate strong performance in identifying highly expressed essential genes but with limited overlap, so we suggest using a combination of these two platforms for highly expressed essential genes; (3) notably, we did not observe a single gene that becomes universally essential across all cancer cell lines.

Indexed as

Genes, EssentialRNA, Small InterferingCell LineCell Line, TumorClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsHumansUnsupervised Machine LearningRNA, Small Interferingconsensus maximizationCRISPRessential genegene expressiongraph-based modelshRNA

Identifiers

PMID39404416
PMCPMC11475473

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.