Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

RNA-seq03:21

RNA-seq

12.5K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
12.5K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

AutoZyme: An Autonomous Agentic Framework to Optimize Bioinformatics Software.

bioRxiv : the preprint server for biologyĀ·2026
Same author

SIRPα ablated iPSC-derived macrophages resist hypophagia and enhance mAb-dependent and CAR-mediated cytotoxicity of solid tumors.

Molecular therapy. OncologyĀ·2026
Same author

Human neural organoid modeling of diffuse midline glioma captures the complexity of patient tumors.

Journal of neuro-oncologyĀ·2026
Same author

Glioblastoma immunotherapy in the context of the aging immune system: a systematic review and meta-analysis.

Journal of neuro-oncologyĀ·2026
Same author

Rapid endothelialization of printed vascular grafts by perivascular niche-circulating endothelial progenitors crosstalk.

Nature communicationsĀ·2025
Same author

CASSIA: a multi-agent large language model for automated and interpretable cell annotation.

Nature communicationsĀ·2025
Same journal

Cross-Domain Transfer Learning from Peptides to Metabolites Using a Multi-Property Fine-Tuned LLM.

Bioinformatics (Oxford, England)Ā·2026
Same journal

Biomedical Concept Recognition with Error-aware Negative-enhanced Ranking Framework.

Bioinformatics (Oxford, England)Ā·2026
Same journal

TEDLH: Domain HMMs for sensitive detection of remote homologues.

Bioinformatics (Oxford, England)Ā·2026
Same journal

PLNFGL: Joint Estimation of Multi-Condition Gene Networks from Single-cell RNA-seq Data.

Bioinformatics (Oxford, England)Ā·2026
Same journal

MCFST: Spatial domain identification method based on multi-view graph convolutional network and graph fusion network.

Bioinformatics (Oxford, England)Ā·2026
Same journal

SpaBiT: Enhancing Spatial Transcriptomics Resolution via Bidirectional Attention Transformers.

Bioinformatics (Oxford, England)Ā·2026
See all related articles

Related Experiment Video

Updated: Mar 27, 2026

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
10:12

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

Published on: January 10, 2019

19.2K

OEFinder: a user interface to identify and visualize ordering effects in single-cell RNA-seq data.

Ning Leng1, Jeea Choi2, Li-Fang Chu1

  • 1Morgridge Institute for Research.

Bioinformatics (Oxford, England)
|January 9, 2016
PubMed
Summary
This summary is machine-generated.

A new artifact, the ordering effect (OE), impacts single-cell RNA sequencing (scRNA-seq) data from Fluidigm C1. OEFinder software identifies these OE genes to prevent biased analysis in scRNA-seq studies.

More Related Videos

Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2
10:10

Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2

Published on: September 18, 2021

42.7K
Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms
10:41

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms

Published on: May 9, 2017

9.7K

Related Experiment Videos

Last Updated: Mar 27, 2026

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
10:12

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

Published on: January 10, 2019

19.2K
Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2
10:10

Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2

Published on: September 18, 2021

42.7K
Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms
10:41

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved Non-model Organisms

Published on: May 9, 2017

9.7K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Single-cell RNA sequencing (scRNA-seq) is a powerful tool for analyzing cellular heterogeneity.
  • An ordering effect (OE) artifact has been identified in scRNA-seq datasets generated by the Fluidigm C1 platform.
  • This OE artifact manifests as significantly increased gene expression in cells captured from specific plate output IDs, potentially biasing downstream analyses.

Purpose of the Study:

  • To develop a statistical method and software tool for identifying the ordering effect (OE) artifact in scRNA-seq data.
  • To provide researchers with a reliable way to detect and mitigate OE-related biases in their Fluidigm C1 datasets.
  • To ensure the accuracy and integrity of scRNA-seq data analysis.

Main Methods:

  • Development of a statistical method to detect the ordering effect (OE) artifact.
  • Creation of OEFinder, an R package with a graphical user interface.
  • Implementation of OEFinder for identifying OE genes in scRNA-seq datasets.

Main Results:

  • OEFinder successfully identifies a sorted list of ordering effect (OE) genes.
  • The software enables users to check for potential artifacts in Fluidigm C1 scRNA-seq data.
  • This facilitates the removal of OE-affected genes, improving data reliability.

Conclusions:

  • The OEFinder tool effectively addresses the ordering effect (OE) artifact in Fluidigm C1 scRNA-seq data.
  • Accurate identification of OE genes prevents biased results in downstream analyses.
  • OEFinder enhances the reliability of scRNA-seq data generated using the Fluidigm C1 platform.