Accurate estimation of cell composition in bulk expression through robust integration of single-cell information
By Brandon Jew, Marcus Alvarez, Elior Rahmani, Zong Miao, Arthur Ko, K. Garske, J. Sul, K. Pietiläinen, P. Pajukanta, Eran Halperin. Nature Communications, 2019
376 citations recorded by the source corpus.
We present Bisque, a tool for estimating cell type proportions in bulk expression. Bisque implements a regression-based approach that utilizes single-cell RNA-seq (scRNA-seq) or single-nucleus RNA-seq (snRNA-seq) data to generate a reference expression profile and learn gene-specific bulk expression transformations to robustly decompose RNA-seq data. These transformations significantly improve decomposition performance compared to existing methods when there is significant technical variation in the generation of the reference profile and observed bulk expression. Importantly, compared to existing methods, our approach is extremely efficient, making it suitable for the analysis of large genomic datasets that are becoming ubiquitous. When applied to subcutaneous adipose and dorsolateral prefrontal cortex expression datasets with both bulk RNA-seq and snRNA-seq data, Bisque replicates previously reported associations between cell type proportions and measured phenotypes across abundant and rare cell types. We further propose an additional mode of operation that merely requires a set of known marker genes. Traditional methods for determining cell type composition lack scalability, while single-cell technologies remain costly and noisy compared to bulk RNA-seq. Here, the authors present a highly efficient tool to measure cellular heterogeneity in bulk expression through robust integration of single-cell information.
Subfields: Epidemiology, Molecular Biology, Physiology
View Paper: https://www.semanticscholar.org/paper/67c90d17f0148313cbe9211413ae0fc0475aa6ce
Citations in the corpus
- Spatially Informed Cell Type Deconvolution for Spatial Transcriptomics (2022, neutral): “21).”