Evidence map›Paper›PMID 19009020›Full record

ArticlePloS one2008

Randomization in laboratory procedure is key to obtaining reproducible microarray results.

Hyuna Yang, Christina A Harrington, Kristina Vartanian, Christopher D Coldren, Rob Hall, Gary A Churchill

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
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

17 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. 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

6 authors at 4 institutions in 1 country.

Hyuna YangThe Jackson Laboratory, Bar Harbor, ME, USA.
Christina A Harrington
Kristina Vartanian
Christopher D Coldren
Rob Hall
Gary A Churchill
Jackson Laboratory · USOregon Health & Science University · USUniversity of Colorado Health · USUniversity of Washington · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Systems Genetic Analysis of Multi-parent CrossesR01GM070683 · NIGMS · JACKSON LABORATORY · PI BROMAN, KARL W, CHURCHILL, GARY A · 2004 to 2022
$6.8M
Expression Analysis to Study Disease PathogenesisR01HL072340 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI GERACI, MARK W · 2002 to 2005
$3.0M
Microarray Program for NHLBI InvestigatorsR01HL072321 · NHLBI · OREGON HEALTH AND SCIENCE UNIVERSITY · PI BAGBY, GROVER CARLTON · 2002 to 2005
$2.9M
NCI NIH HHS CA034196NCI NIH HHS P30 CA034196NHLBI NIH HHS R01 HL072321NHLBI NIH HHS R01 HL72321NHLBI NIH HHS R01 HL7234001NIGMS NIH HHS GM070683NIGMS NIH HHS R01 GM070683
6 · The paper itself

Abstract

The quality of gene expression microarray data has improved dramatically since the first arrays were introduced in the late 1990s. However, the reproducibility of data generated at multiple laboratory sites remains a matter of concern, especially for scientists who are attempting to combine and analyze data from public repositories. We have carried out a study in which a common set of RNA samples was assayed five times in four different laboratories using Affymetrix GeneChip arrays. We observed dramatic differences in the results across laboratories and identified batch effects in array processing as one of the primary causes for these differences. When batch processing of samples is confounded with experimental factors of interest it is not possible to separate their effects, and lists of differentially expressed genes may include many artifacts. This study demonstrates the substantial impact of sample processing on microarray analysis results and underscores the need for randomization in the laboratory as a means to avoid confounding of biological factors with procedural effects.

Indexed as

AnimalsChromosomes, MammalianCluster AnalysisFemaleGene Expression ProfilingGene Expression RegulationLaboratoriesMaleMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisPrincipal Component AnalysisRandom AllocationReproducibility of ResultsSex Characteristics

Identifiers

PMID19009020
PMCPMC2579585
OpenAlexW1996353320

What OpenQuestion 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 OpenQuestion graph.