More accurate estimation of cell composition in bulk expression through robust integration of single-cell information
Bibliographic record
Abstract
Motivation: The rapid single-cell transcriptomic technology developments have led to an increasing interest in cellular heterogeneity within cell populations. Although cell-type proportions can be obtained directly from single-cell RNA sequencing (scRNA-seq), it is costly and not feasible in every study. Alternatively, with fewer experimental complications, cell-type compositions are characterized from bulk RNA-seq data. Many computational tools have been developed and reported in the literature. However, they fail to appropriately incorporate the covariance structures in both scRNA-seq and bulk RNA-seq datasets in use. Results: We present a covariance-based single-cell decomposition (CSCD) method that estimates cell-type proportions in bulk data through building a reference expression profile based on a single-cell data, and learning gene-specific bulk expression transformations using a constrained linear inverse model. The approach is similar to Bisque, a cell-type decomposition method that was recently developed. Bisque is limited to a univariate model, thus unable to incorporate gene-gene correlations into the analysis. We introduce a more advanced model that successfully incorporates the covariance structures in both scRNA-seq and bulk RNA-seq datasets into the analysis, and fixes the collinearity issue by utilizing a linear shrinkage estimation of the corresponding covariance matrices. We applied CSCD to several publicly available datasets and measured the performance of CSCD, Bisque and six other common methods in the literature. Our results indicate that CSCD is more accurate and comprehensive than most of the existing methods. Availability and implementation: The R package is available on https://github.com/empiricalbayes/CSCDRNA.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.002 | 0.004 |
| Meta-epidemiology (narrow) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.001 |
| Bibliometrics | 0.001 | 0.001 |
| Science and technology studies | 0.000 | 0.001 |
| Scholarly communication | 0.001 | 0.001 |
| Open science | 0.001 | 0.001 |
| Research integrity | 0.001 | 0.001 |
| Insufficient payload (model declined to judge) | 0.001 | 0.001 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".