Risk-conscious correction of batch effects: maximising information extraction from high-throughput genomic datasets
Autor: | Yalchin Oytam, Konsta Duesing, Fariborz Sobhanmanesh, Joshua C. Bowden, Jason P. Ross, Megan J. Osmond-McLeod |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Computer science ComBat Information Storage and Retrieval Guided PCA computer.software_genre Biochemistry Set (abstract data type) 03 medical and health sciences 0302 clinical medicine Batch effects Structural Biology Humans Molecular Biology Throughput (business) Statistical hypothesis testing Principal Component Analysis Sequence Analysis RNA Noise (signal processing) Methodology Article Applied Mathematics Singular value decomposition Genomics Measurement noise Computer Science Applications Information extraction 030104 developmental biology 030220 oncology & carcinogenesis Benchmark (computing) High-throughput genomic data Data mining computer |
Zdroj: | BMC Bioinformatics |
ISSN: | 1471-2105 |
DOI: | 10.1186/s12859-016-1212-5 |
Popis: | Background Batch effects are a persistent and pervasive form of measurement noise which undermine the scientific utility of high-throughput genomic datasets. At their most benign, they reduce the power of statistical tests resulting in actual effects going unidentified. At their worst, they constitute confounds and render datasets useless. Attempting to remove batch effects will result in some of the biologically meaningful component of the measurement (i.e. signal) being lost. We present and benchmark a novel technique, called Harman. Harman maximises the removal of batch noise with the constraint that the risk of also losing biologically meaningful component of the measurement is kept to a fraction which is set by the user. Results Analyses of three independent publically available datasets reveal that Harman removes more batch noise and preserves more signal at the same time, than the current leading technique. Results also show that Harman is able to identify and remove batch effects no matter what their relative size compared to other sources of variation in the dataset. Of particular advantage for meta-analyses and data integration is Harman’s superior consistency in achieving comparable noise suppression - signal preservation trade-offs across multiple datasets, with differing number of treatments, replicates and processing batches. Conclusion Harman’s ability to better remove batch noise, and better preserve biologically meaningful signal simultaneously within a single study, and maintain the user-set trade-off between batch noise rejection and signal preservation across different studies makes it an effective alternative method to deal with batch effects in high-throughput genomic datasets. Harman is flexible in terms of the data types it can process. It is available publically as an R package (https://bioconductor.org/packages/release/bioc/html/Harman.html), as well as a compiled Matlab package (http://www.bioinformatics.csiro.au/harman/) which does not require a Matlab license to run. Electronic supplementary material The online version of this article (doi:10.1186/s12859-016-1212-5) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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