4.7 Article

Balancing the transcriptome: leveraging sample similarity to improve measures of gene specificity

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 23, Issue 5, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbac158

Keywords

gene specificity; similarity; weighting; transcriptomics; GTEx

Funding

  1. National Institutes of Health [DP5OD024579, T32HG002536, T32LM012424]

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Quantifying the specificity of gene expression is crucial for studying the etiology of genetic diseases, but it remains challenging due to sample similarity. This study demonstrates that incorporating sample similarity information improves the stability of specificity estimates and provides more robust measures for downstream analyses.
The spatial and temporal domain of a gene's expression can range from ubiquitous to highly specific. Quantifying the degree to which this expression is unique to a specific tissue or developmental timepoint can provide insight into the etiology of genetic diseases. However, quantifying specificity remains challenging as measures of specificity are sensitive to similarity between samples in the sample set. For example, in the Gene-Tissue Expression project (GTEx), brain subregions are overrepresented at 13 of 54 (24%) unique tissues sampled. In this dataset, existing specificity measures have a decreased ability to identify genes specific to the brain relative to other organs. To solve this problem, we leverage sample similarity information to weight samples such that overrepresented tissues do not have an outsized effect on specificity estimates. We test this reweighting procedure on 4 measures of specificity, Z-score, Tau, Tsi and Gini, in the GTEx data and in single cell datasets for zebrafish and mouse. For all of these measures, incorporating sample similarity information to weight samples results in greater stability of sets of genes called as specific and decreases the overall variance in the change of specificity estimates as sample sets become more unbalanced. Furthermore, the genes with the largest improvement in their specificity estimate's stability are those with functions related to the overrepresented sample types. Our results demonstrate that incorporating similarity information improves specificity estimates' stability to the choice of the sample set used to define the transcriptome, providing more robust and reproducible measures of specificity for downstream analyses.

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