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 quantitative evaluation of SAGE.

J Stollberg1, J Urschitz, Z Urban

  • 1Pacific Biomedical Research Center, University of Hawai'i at Manoa, Honolulu, Hawaii 96822, USA. jesse@pbrc.hawaii.edu

Genome Research
|August 25, 2000
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

Using diffusion MRI data acquired with ultra-high gradient strength to improve tractography in routine-quality data.

NeuroImage·2021
Same author

Constitutively active TrkB confers an aggressive transformed phenotype to a neural crest-derived cell line.

Oncogene·2013
Same author

In vitro translation of messenger RNA in a wheat germ extract cell-free system.

Methods in molecular biology (Clifton, N.J.)·2011
Same author

In vitro translation of messenger RNA in a rabbit reticulocyte lysate cell-free system.

Methods in molecular biology (Clifton, N.J.)·2011
Same author

Immunoprecipitation of in vitro translation products with protein a bound to sepharose.

Methods in molecular biology (Clifton, N.J.)·2011
Same author

A novel fibrotic disorder associated with increased dermal fibroblast proliferation and downregulation of genes of the microfibrillar network.

The British journal of dermatology·2010
Same journal

Complete sequencing of medaka genomes reveals the architecture of centromeric satellites, giant mobile elements, and sex chromosomes.

Genome research·2026
Same journal

Convergence and conflict among telomere specialized transposons across 60 million years of Drosophilid evolution.

Genome research·2026
Same journal

A unified analysis of cell type- and trajectory-associated pathways in single-cell data using Phoenix.

Genome research·2026
Same journal

Resf1 is required for proper placental development and configuration of trophoblast cell-specific heterochromatin.

Genome research·2026
Same journal

Telomere-driven replicative crisis is driven by large-scale changes in genomic architecture.

Genome research·2026
Same journal

Spatially informed reference-free cell-type deconvolution for spatial transcriptomics with SpatialCD.

Genome research·2026
See all related articles

Serial Analysis of Gene Expression (SAGE) provides gene expression data but has inherent biases. This study introduces a mathematical method to correct these biases, offering more accurate gene expression and copy number estimates.

Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • Serial Analysis of Gene Expression (SAGE) is a powerful technique for quantifying mRNA transcripts.
  • SAGE experiments are subject to inherent biases including sampling, sequencing, nonuniqueness, and nonrandomness of tag sequences.
  • Accurate estimation of gene number and transcript copy frequencies is crucial for understanding gene expression.

Purpose of the Study:

  • To develop a mathematical framework for maximum likelihood estimation of gene number and transcript copy frequencies.
  • To account for inherent biases in SAGE experimental data.
  • To assess the uniqueness of tag sequences within a genome.

Main Methods:

  • Development of a maximum likelihood estimation model.

Related Experiment Videos

  • Incorporation of mathematical corrections for SAGE-specific biases.
  • Analysis of tag sequence uniqueness in relation to genome size.
  • Main Results:

    • The proposed method yields gene expression and copy number estimates that differ significantly from raw SAGE data.
    • Mathematical biases inherent in SAGE experiments can be effectively addressed.
    • Tag sequence uniqueness is generally probable but cannot be assumed in larger genomes.

    Conclusions:

    • Maximum likelihood estimation provides a more accurate representation of true genomic expression from SAGE data.
    • Correcting for experimental biases is essential for reliable gene expression analysis.
    • The assumption of tag uniqueness requires careful consideration, especially in complex genomes.