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 Experiment Videos

A simple method for assessing sample sizes in microarray experiments.

Robert Tibshirani1

  • 1Health Research & Policy, Stanford University, Stanford, CA 94305, USA. tibs@stanford.edu

BMC Bioinformatics
|March 4, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Cell Cycle Sensing Shapes Human T Cell Fate and Exhaustion Programs.

bioRxiv : the preprint server for biology·2026
Same author

Wavelet Decomposition-Based Genomic Analysis of the Human Electrocardiogram.

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

Structure-preserving multivariate hypothesis testing for mass spectrometry imaging and single-cell data.

Bioinformatics (Oxford, England)·2026
Same author

Temporal and spatial composition of the tumor microenvironment predicts response to immune checkpoint inhibition in metastatic TNBC.

Nature cancer·2026
Same author

Prognostic pan-cancer and single-cancer models: A large-scale analysis using a real-world clinico-genomic database.

PloS one·2026
Same author

Glaucoma Classification Through SSVEP-Derived ON- and OFF-Pathway Features.

Translational vision science & technology·2026
Same journal

OpenIMC: an open-source platform for analyzing single-cell and spatial proteomics by imaging mass cytometry.

BMC bioinformatics·2026
Same journal

NAP: an open source pipeline for cross-domain microbiome profiling using Nanopore sequencing-derived amplicon data.

BMC bioinformatics·2026
Same journal

SurvGME: an R package for survival analysis with graphical and measurement error models.

BMC bioinformatics·2026
Same journal

SimMapNet: a Bayesian framework for gene regulatory network inference using gene ontology similarities as external hint.

BMC bioinformatics·2026
Same journal

Dual channel drug-drug interactions extraction based on cross attention.

BMC bioinformatics·2026
Same journal

FeSseqdb: a curated sequence-level database and interpretable machine learning framework for identifying iron-sulfur proteins.

BMC bioinformatics·2026
See all related articles

This study presents a straightforward method for determining sample size in microarray experiments. It helps estimate gene-specific power and error rates, aiding researchers in planning robust studies.

Area of Science:

  • Bioinformatics
  • Genomics
  • Statistical Genetics

Background:

  • Microarray experiments are crucial for high-throughput gene expression analysis.
  • Determining appropriate sample size is essential for the statistical power and reliability of microarray studies.
  • Existing methods for sample size calculation can be complex or lack direct applicability to gene-specific metrics.

Purpose of the Study:

  • To introduce a simple and practical method for assessing sample size requirements in microarray experiments.
  • To provide a framework for estimating key statistical parameters relevant to gene discovery.
  • To demonstrate the adaptability of the proposed method to various experimental designs and response variables.

Main Methods:

  • The method utilizes output from permutation-based analyses, such as those from the Significance Analysis of Microarrays (SAM) package.

Related Experiment Videos

  • It involves estimating the false discovery rate (FDR) and false negative rate (FNR) for a list of genes across different sample sizes.
  • These estimates are directly interpretable as per-gene power and type I error rates.
  • Main Results:

    • The proposed method provides estimates of false discovery and false negative rates, which correspond to gene-specific power and type I error.
    • It allows researchers to evaluate the impact of different sample sizes on the detection of significant genes.
    • The approach is shown to be applicable to other response variables, including survival outcomes.

    Conclusions:

    • The presented method offers a useful tool for sample size assessment in the context of microarray experiments.
    • It facilitates informed decisions regarding the number of samples needed to achieve desired statistical power.
    • The method's flexibility extends its utility to a broader range of genomic and statistical applications.