normalization in cross meta-analysis
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4.5 years ago

Dear all,

I am trying to perform a meta-analysis using microarray data of 6 datasets with different platforms (Illumina HumanHT-12 V4.0 expression beadchip, Affymetrix Human Exon 1.0 ST Array, Affymetrix Human Gene 1.0 ST Array).

My question is about the first step of meta-analysis which is data normalization (before merging the data and remove the batch effect), may I normalize all of the dataset simultaneous (for example using the LIMMA package)? Or must be normalized them separately? Which way is correct and the best way?

Thank you in advance.

R • 1.6k views
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4.5 years ago
JC 13k

It is never recommended to merge raw data from different technologies, so it's better to normalize/analyze the data separately and then merge your results.

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Thank you for your answer, but in some studies (below links) different microarray platforms have been integrated, the created batch effects after merging data are removed (for example by ComBat function in sva package).

https://www.biorxiv.org/content/10.1101/059600v1.full#disqus_thread

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697344/

https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0194844

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996376/

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  1. Normalization is before merge at probeset level https://www.biorxiv.org/content/biorxiv/early/2016/06/18/059600/F1.medium.gif
  2. "The first step in the methodology for microarray data is to put together all the selected series, independently of their technology (Affimetrix or Illumina). Consequently, a quality analysis assessment was performed across the series, in order to detect and consequently remove any possible outlier" -> so they are normalizing before merge the data
  3. The preprocessing is before merge at the gene level https://journals.plos.org/plosone/article/figure/image?size=inline&id=info:doi/10.1371/journal.pone.0194844.g001
  4. "One major limitation of existing cross-platform normalization is that they require that every treatment group or sample type be represented on each platform to allow differentiation of treatment effects from platform effects. Furthermore, cross-platform normalization methods do not guarantee elimination of laboratory or batch effects across experiments"
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