Evidence map›Paper›PMID 26608184›Full record

ArticleArchives of toxicology2015

Identification of sample annotation errors in gene expression datasets.

Miriam Lohr, Birte Hellwig, Karolina Edlund, Johanna S M Mattsson, Johan Botling, Marcus Schmidt, Jan G Hengstler, Patrick Micke, Jörg Rahnenführer

Abstract read
In one paragraph

Article in Archives of toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  20. HYSYS: have you swapped your samples?Bioinformatics (Oxford, England) · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Miriam LohrDepartment of Statistics, TU Dortmund University, Vogelpothsweg 87, 44227, Dortmund, Germany.
Birte HellwigDepartment of Statistics, TU Dortmund University, Vogelpothsweg 87, 44227, Dortmund, Germany.
Karolina EdlundLeibniz Research Centre for Working Environment and Human Factors (IfADo) at Dortmund TU, Dortmund, Germany.
Johanna S M MattssonDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Johan BotlingDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Marcus SchmidtDepartment of Obstetrics and Gynecology, University Hospital, Mainz, Germany.
Jan G HengstlerLeibniz Research Centre for Working Environment and Human Factors (IfADo) at Dortmund TU, Dortmund, Germany.
Patrick MickeDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Jörg RahnenführerDepartment of Statistics, TU Dortmund University, Vogelpothsweg 87, 44227, Dortmund, Germany. rahnenfuehrer@statistik.tu-dortmund.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The comprehensive transcriptomic analysis of clinically annotated human tissue has found widespread use in oncology, cell biology, immunology, and toxicology. In cancer research, microarray-based gene expression profiling has successfully been applied to subclassify disease entities, predict therapy response, and identify cellular mechanisms. Public accessibility of raw data, together with corresponding information on clinicopathological parameters, offers the opportunity to reuse previously analyzed data and to gain statistical power by combining multiple datasets. However, results and conclusions obviously depend on the reliability of the available information. Here, we propose gene expression-based methods for identifying sample misannotations in public transcriptomic datasets. Sample mix-up can be detected by a classifier that differentiates between samples from male and female patients. Correlation analysis identifies multiple measurements of material from the same sample. The analysis of 45 datasets (including 4913 patients) revealed that erroneous sample annotation, affecting 40 % of the analyzed datasets, may be a more widespread phenomenon than previously thought. Removal of erroneously labelled samples may influence the results of the statistical evaluation in some datasets. Our methods may help to identify individual datasets that contain numerous discrepancies and could be routinely included into the statistical analysis of clinical gene expression data.

Indexed as

Databases, GeneticFemaleGene Expression ProfilingHumansMaleOligonucleotide Array Sequence AnalysisReproducibility of ResultsTranscriptomeGene expressionMale–female classifierMicroarrayMisannotationQuality control

Identifiers

PMID26608184
PMCPMC4673097

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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.