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

DNA Microarrays02:34

DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

You might also read

Related Articles

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

Sort by
Same author

Real-World Associations of KidneyIntelX Risk Stratification With Guideline-Directed Therapy, Kidney Outcomes, and Metabolic Trajectories in Early Diabetic Kidney Disease.

Diabetes, obesity & metabolism·2026
Same author

BIRC3 (Encoding Cellular Inhibitor of Apoptosis Protein 2) Variants Result in Dysregulated Receptor-Interacting Protein Kinase 1 Signaling Leading to Increased Epithelial Cell Death and Are Associated With Monogenic Crohn's Disease.

Gastroenterology·2026
Same author

Low-Effort Respiratory Function Estimation with a Soft Wearable Digital Spirometry Patch.

Biosensors·2026
Same author

Tryptophan pathway metabotypes associate with disease activity and immune-metabolic dysfunction in inflammatory bowel disease.

medRxiv : the preprint server for health sciences·2026
Same author

Clinical and Imaging Abnormalities Associated With Inducible Ventricular Arrhythmias During Electrophysiologic Study in Patients With Cardiac Sarcoidosis and Mildly Impaired Left Ventricular Function.

Journal of the American Heart Association·2026
Same author

SleepJEPA: Learning the latent world of sleep with at-home sleep data to estimate disease risk.

medRxiv : the preprint server for health sciences·2026

Related Experiment Video

Updated: Jul 13, 2026

Using Microarrays to Interrogate Microenvironmental Impact on Cellular Phenotypes in Cancer
08:20

Using Microarrays to Interrogate Microenvironmental Impact on Cellular Phenotypes in Cancer

Published on: May 21, 2019

Comparing microarray studies.

Mayte Suárez-Fariñas1, Marcelo O Magnasco

  • 1Center for Studies in Physics and Biology, The Rockefeller University, New York, NY, USA.

Methods in Molecular Biology (Clifton, N.J.)
|July 20, 2007
PubMed
Summary

Comparing microarray studies requires careful consideration of technology, protocols, and lab variability. This guide offers methods and pitfalls for reliable data integration and analysis.

Area of Science:

  • Bioinformatics
  • Genomics
  • Biostatistics

Background:

  • Microarray technology enables large-scale gene expression profiling.
  • Integrating data from diverse microarray studies presents significant challenges.
  • Variability in experimental design and analysis can impact study agreement.

Purpose of the Study:

  • To provide a practical guide for comparing and integrating different microarray studies.
  • To identify key factors influencing agreement between microarray studies.
  • To offer methods and highlight common pitfalls in microarray data analysis.

Main Methods:

  • Discussion of factors affecting study agreement: technology, platforms, statistical criteria, protocols, lab variability.
  • Presentation of methods for comparing and refining microarray study integration.

More Related Videos

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning
09:27

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning

Published on: March 15, 2011

Performing Custom MicroRNA Microarray Experiments
07:04

Performing Custom MicroRNA Microarray Experiments

Published on: October 28, 2011

Related Experiment Videos

Last Updated: Jul 13, 2026

Using Microarrays to Interrogate Microenvironmental Impact on Cellular Phenotypes in Cancer
08:20

Using Microarrays to Interrogate Microenvironmental Impact on Cellular Phenotypes in Cancer

Published on: May 21, 2019

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning
09:27

DNA Microarrays: Sample Quality Control, Array Hybridization and Scanning

Published on: March 15, 2011

Performing Custom MicroRNA Microarray Experiments
07:04

Performing Custom MicroRNA Microarray Experiments

Published on: October 28, 2011

  • Illustrative example case study.
  • Main Results:

    • Identification of critical variables (technology, protocols, lab variability) impacting microarray study comparability.
    • Detailed methods for robust data integration and comparison.
    • Common pitfalls in microarray analysis are highlighted.

    Conclusions:

    • Careful consideration of technical and analytical factors is crucial for successful microarray study comparison.
    • Standardized approaches and awareness of potential pitfalls enhance the reliability of integrated microarray data.
    • This guide facilitates more accurate and meaningful cross-study analyses in genomics.