SSMD
SSMD estimates dataset-specific cell-type signature genes and relative cell-type proportions from mouse transcriptomic, DNA methylation, and ATAC-seq datasets to enable deconvolution of complex mouse tissues.
Key Features:
- Non-parametric dataset-specific signature identification: Employs a novel non-parametric approach to identify dataset-specific cell-type signature genes tailored to each experimental condition.
- Community detection for cell-type and marker refinement: Uses a community detection method to establish and refine cell types and their marker genes across variable genetic and phenotypic backgrounds.
- Constrained matrix decomposition for proportion estimation: Applies constrained matrix decomposition to determine relative cell-type proportions across diverse experimental platforms.
Scientific Applications:
- Handling variable cell types and markers: Manages variability in cell types and marker genes arising from different genotypic and phenotypic conditions in mouse models.
- Cross-platform deconvolution: Operates across diverse experimental platforms to maintain consistent deconvolution performance regardless of data source.
- Small-sample studies: Functions with limited training data, enabling application in studies with small sample sizes.
- Comprehensive cell-type estimation: Estimates proportions for over 35 cell types across systems including blood, inflammatory tissues, the central nervous system, and hematopoietic systems.
Methodology:
SSMD implements a semi-supervised framework combining non-parametric identification of dataset-specific signature genes, community detection to define and refine cell types and markers, and constrained matrix decomposition to estimate relative cell-type proportions; it is applied to transcriptomics, DNA methylation, and ATAC-seq data.
Topics
Details
- Programming Languages:
- R
- Added:
- 1/18/2021
- Last Updated:
- 2/21/2021
Operations
Publications
Lu X, Tu S, Chang W, Wan C, Wang J, Zang Y, Ramdas B, Kapur R, Lu X, Cao S, Zhang C. SSMD: A semi-supervised approach for a robust cell type identification and deconvolution of mouse transcriptomics data. Unknown Journal. 2020. doi:10.1101/2020.09.22.309278.