Evidence map›Paper›PMID 30423059›Full record

ArticleBioinformatics (Oxford, England)2018

An ontology-based method for assessing batch effect adjustment approaches in heterogeneous datasets.

Florian Schmidt, Markus List, Engin Cukuroglu, Sebastian Köhler, Jonathan Göke, Marcel H Schulz

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Florian SchmidtMax Planck Institute for Informatics, Saarland Informatics Campus, Saarbrücken, Germany.
Markus ListMax Planck Institute for Informatics, Saarland Informatics Campus, Saarbrücken, Germany.
Engin CukurogluGenome Institute of Singapore, Computational Genomics and Transcriptomics, Singapore.
Sebastian KöhlerBerlin Institute of Health (BIH), Berlin, Germany.
Jonathan GökeGenome Institute of Singapore, Computational Genomics and Transcriptomics, Singapore.
Marcel H SchulzMax Planck Institute for Informatics, Saarland Informatics Campus, Saarbrücken, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: International consortia such as the Genotype-Tissue Expression (GTEx) project, The Cancer Genome Atlas (TCGA) or the International Human Epigenetics Consortium (IHEC) have produced a wealth of genomic datasets with the goal of advancing our understanding of cell differentiation and disease mechanisms. However, utilizing all of these data effectively through integrative analysis is hampered by batch effects, large cell type heterogeneity and low replicate numbers. To study if batch effects across datasets can be observed and adjusted for, we analyze RNA-seq data of 215 samples from ENCODE, Roadmap, BLUEPRINT and DEEP as well as 1336 samples from GTEx and TCGA. While batch effects are a considerable issue, it is non-trivial to determine if batch adjustment leads to an improvement in data quality, especially in cases of low replicate numbers. Results: We present a novel method for assessing the performance of batch effect adjustment methods on heterogeneous data. Our method borrows information from the Cell Ontology to establish if batch adjustment leads to a better agreement between observed pairwise similarity and similarity of cell types inferred from the ontology. A comparison of state-of-the art batch effect adjustment methods suggests that batch effects in heterogeneous datasets with low replicate numbers cannot be adequately adjusted. Better methods need to be developed, which can be assessed objectively in the framework presented here. Availability and implementation: Our method is available online at https://github.com/SchulzLab/OntologyEval. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Datasets as TopicData AccuracyGene OntologyGenome, HumanGenomicsHumansRNASequence Analysis, RNARNA

Identifiers

PMID30423059
PMCPMC6129283

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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.