Sstack

Sstack integrates heterogeneous genomic feature sets to enable predictive modeling when subsets of genomic features are missing across samples.


Key Features:

  • Heterogeneous Data Integration: Handles scenarios where different subsets of genomic features are missing in parts of a dataset, enabling analysis of incomplete datasets without compromising model integrity.
  • Sequential Addition of Samples and Features: Supports sequential addition of samples and features to accommodate incremental data collection and dynamic information integration.
  • Improved Prediction Accuracy: Stacks genomic datasets to improve predictive accuracy, as demonstrated in drug sensitivity prediction using the Cancer Cell Line Encyclopedia (CCLE).
  • R Package Implementation: Implemented as an R package for use within R-based computational workflows.

Scientific Applications:

  • Drug Sensitivity Prediction: Enhances accuracy of drug response predictions, demonstrated using CCLE data to inform precision medicine analyses.
  • Genomic Data Analysis: Enables analysis of complex genomic datasets with missing features to support biological insight and downstream modeling.

Methodology:

Sstack stacks different genomic feature sets to create a unified model that compensates for missing data and supports the sequential addition of samples and features.

Topics

Details

License:
GPL-3.0
Maturity:
Mature
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
5/25/2019
Last Updated:
11/25/2024

Operations

Publications

Matlock K, Rahman R, Ghosh S, Pal R. <i>Sstack</i>: an R package for stacking with applications to scenarios involving sequential addition of samples and features. Bioinformatics. 2019;35(17):3143-3145. doi:10.1093/bioinformatics/btz010. PMID:30649230. PMCID:PMC6736036.

PMID: 30649230
PMCID: PMC6736036
Funding: - National Institutes of Health: R01GM122084