Correction of a widespread bias in pooled chemical genomics screens improves their interpretability

Chemical genomics is a powerful and increasingly accessible technique to probe gene function, gene-gene interactions, and antibiotic synergies and antagonisms. Indeed, multiple large-scale pooled datasets in diverse organisms have been published. Here, we identify an artifact arising from uncorrected differences in the number of cell doublings between experiments within such datasets. We demonstrate that this artifact is widespread, show how it causes spurious gene-gene and drug-drug correlations, and present a simple but effective post hoc method for removing its effects. Using several published datasets, we demonstrate that this correction removes spurious correlations between genes and conditions, improving data interpretability and revealing new biological insights. Finally, we determine experimental factors that predispose a dataset for this artifact and suggest a set of experimental and computational guidelines for performing pooled chemical genomics experiments that will maximize the potential of this powerful technique.

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Publication Details

Journal
Molecular Systems Biology
Published
2024-09-30
DOI
https://doi.org/10.1038/s44320-024-00069-y
Citations
5
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
1.17

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article

Correction of a widespread bias in pooled chemical genomics screens improves their interpretability

Lili M. Kim, Carol A. Gross, Horia Todor
5 citations
Molecular Systems Biology
CRISPR and Genetic Engineering
1.17
article

Correction of a widespread bias in pooled chemical genomics screens improves their interpretability

Lili M. Kim, Carol A. Gross, Horia Todor
article en
5 citations

Abstract

Chemical genomics is a powerful and increasingly accessible technique to probe gene function, gene-gene interactions, and antibiotic synergies and antagonisms. Indeed, multiple large-scale pooled datasets in diverse organisms have been published. Here, we identify an artifact arising from uncorrected differences in the number of cell doublings between experiments within such datasets. We demonstrate that this artifact is widespread, show how it causes spurious gene-gene and drug-drug correlations, and present a simple but effective post hoc method for removing its effects. Using several published datasets, we demonstrate that this correction removes spurious correlations between genes and conditions, improving data interpretability and revealing new biological insights. Finally, we determine experimental factors that predispose a dataset for this artifact and suggest a set of experimental and computational guidelines for performing pooled chemical genomics experiments that will maximize the potential of this powerful technique.

Molecular Systems BiologyVol. 20(11)
QB3 (US), University of California, San Francisco (US)
National Institutes of Health
Openalex Percentile: Top 22%
CRISPR and Genetic Engineering
1.17
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