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This study establishes that recovering causal gene regulatory networks from bulk expression data is theoretically limited to linear aggregations with affine structural equations. Empirical analysis of multiple datasets reveals that gene regulatory functions typically deviate from these linearity assumptions, casting doubt on the validity of existing causal inference methods applied to bulk data. Practitioners should exercise caution when interpreting causal relations derived from aggregated expression profiles without incorporating strong, specific constraints.
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On the Recoverability of Causal Relations from Bulk Gene Expression Data

arXiv3 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2606.00568v2 Announce Type: replace Abstract: Bulk gene expression profiling, which aggregates pooled RNA across cells within a biological sample, remains important in the single-cell era because it is typically less noisy, more sensitive, and more cost-effective than single-cell assays. Accordingly, a growing body of computational methods seeks to recover causal relations among genes from bulk expression data. However, aggregation is a lossy, non-invertible coarsening of the underlying cellular system, and it remains unclear whether and under what conditions causal relations are recoverable from aggregated bulk gene expression data. To answer this, we formalize recoverability under aggregation through two notions of consistency: functional-form consistency and conditional-independence consistency. We then derive necessary and sufficient conditions for recoverability, showing that these properties are preserved only under linear aggregations (e.g., sum/mean) coupled with affine structural equations. To assess the practical plausibility of these conditions, analyses of four bulk and four single-cell gene expression datasets further reveal that the estimated pairwise regulatory functions among genes deviate from linearity in both data types, providing limited empirical support for the linearity assumptions required for recoverability. Together, these results caution against recovering causal relations from aggregated bulk expression data without strong additional assumptions.

Abstract:Bulk gene expression profiling, which aggregates pooled RNA across cells within a biological sample, remains important in the single-cell era because it is typically less noisy, more sensitive, and more cost-effective than single-cell assays. Accordingly, a growing body of computational methods seeks to recover causal relations among genes from bulk expression data. However, aggregation is a lossy, non-invertible coarsening of the underlying cellular system, and it remains unclear whether and under what conditions causal relations are recoverable from aggregated bulk gene expression data. To answer this, we formalize recoverability under aggregation through two notions of consistency: functional-form consistency and conditional-independence consistency. We then derive necessary and sufficient conditions for recoverability, showing that these properties are preserved only under linear aggregations (e.g., sum/mean) coupled with affine structural equations. To assess the practical plausibility of these conditions, analyses of four bulk and four single-cell gene expression datasets further reveal that the estimated pairwise regulatory functions among genes deviate from linearity in both data types, providing limited empirical support for the linearity assumptions required for recoverability. Together, these results caution against recovering causal relations from aggregated bulk expression data without strong additional assumptions.

Machine Learning (cs.LG); Genomics (q-bio.GN)

arXiv:2606.00568 [cs.LG]

(or arXiv:2606.00568v2 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2606.00568 Focus to learn more arXiv-issued DOI via DataCite

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