Evidence map›Paper›PMID 23958724›Full record

ArticleBioinformatics (Oxford, England)2013

A new statistic for identifying batch effects in high-throughput genomic data that uses guided principal component analysis.

Sarah E Reese, Kellie J Archer, Terry M Therneau, Elizabeth J Atkinson, Celine M Vachon, Mariza de Andrade, Jean-Pierre A Kocher, Jeanette E Eckel-Passow

Open access · bronzeAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

83 citing papers in PubMed, 150 citations in OpenAlex.

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  19. Principled and interpretable alignability testing and integration of single-cell data.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  20. Article

23 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Sarah E ReeseDepartment of Biostatistics, Biostatistics Shared Resource Core, VCU Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23284, USA, Division of Biomedical Statistics and Informatics and Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
Kellie J Archer
Terry M Therneau
Elizabeth J Atkinson
Celine M Vachon
Mariza de Andrade
Jean-Pierre A Kocher
Jeanette E Eckel-Passow
Virginia Commonwealth University · USMayo Clinic · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
Genomic Predictors of Arteriosclerosis in HypertensivesR01HL087660 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARDIA, SHARON L · 2007 to 2009
$5.1M
Identifying Genes for Mammographic Breast DensityR01CA128931 · NCI · MAYO CLINIC ROCHESTER · PI VACHON, CELINE M · 2008 to 2012
$2.7M
Risk factors for breast cancer molecular subtypesR01CA140286 · NCI · MAYO CLINIC ROCHESTER · PI KERLIKOWSKE, KARLA M, VACHON, CELINE M · 2010 to 2014
$2.6M
Integration of Mixtures Toxicology, Toxicogenomics, and StatisticsT32ES007334 · NIEHS · VIRGINIA COMMONWEALTH UNIVERSITY · PI WHEELER, DAVID CHARLES · 2002 to 2018
$2.5M
NCI NIH HHS CA140286NCI NIH HHS P30 CA015083NCI NIH HHS P30 CA016059NCI NIH HHS R01 CA128931NCI NIH HHS R01 CA140286NHLBI NIH HHS R01 HL87660NIEHS NIH HHS T32 ES007334
6 · The paper itself

Abstract

motivationBatch effects are due to probe-specific systematic variation between groups of samples (batches) resulting from experimental features that are not of biological interest. Principal component analysis (PCA) is commonly used as a visual tool to determine whether batch effects exist after applying a global normalization method. However, PCA yields linear combinations of the variables that contribute maximum variance and thus will not necessarily detect batch effects if they are not the largest source of variability in the data.

resultsWe present an extension of PCA to quantify the existence of batch effects, called guided PCA (gPCA). We describe a test statistic that uses gPCA to test whether a batch effect exists. We apply our proposed test statistic derived using gPCA to simulated data and to two copy number variation case studies: the first study consisted of 614 samples from a breast cancer family study using Illumina Human 660 bead-chip arrays, whereas the second case study consisted of 703 samples from a family blood pressure study that used Affymetrix SNP Array 6.0. We demonstrate that our statistic has good statistical properties and is able to identify significant batch effects in two copy number variation case studies.

conclusionWe developed a new statistic that uses gPCA to identify whether batch effects exist in high-throughput genomic data. Although our examples pertain to copy number data, gPCA is general and can be used on other data types as well. AVAILABILITY AND IMPLEMENTATION: The gPCA R package (Available via CRAN) provides functionality and data to perform the methods in this article. CONTACT: reesese@vcu.edu

Indexed as

Principal Component AnalysisData Interpretation, StatisticalDNA Copy Number VariationsGenomicsHumansOligonucleotide Array Sequence AnalysisPolymorphism, Single Nucleotide

Identifiers

PMID23958724
PMCPMC3810845
OpenAlexW2118521406

What OpenQuestion holds

Textmetadata
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.