compSPOT
compSPOT identifies and compares significantly mutated genomic hotspots to establish cancer risk markers.
Key Features:
- Hotspot Identification: Establishes significantly mutated genomic regions with increased sensitivity to acquiring mutations.
- Comparative Analysis: Compares hotspot mutation burden between samples.
- Exploratory Data Analysis: Analyzes correlations between hotspot mutation burden and personal risk factors for cancer, including age, gender, and history of carcinogen exposure.
Scientific Applications:
- Cancer Risk Prediction: Identifies robust genomic markers to help establish cancer risk based on mutation-sensitive genomic regions.
- Prognosis Assessment: Evaluates how the frequency and location of mutations in clonal cell groups may predict prognosis.
- Risk Factor Correlation: Investigates relationships between hotspot mutation burden and carcinogen exposure history.
Methodology:
The package contains multiple functions to establish significantly mutated hotspots, compare hotspot mutation burden between samples, and perform exploratory data analysis of correlations with personal risk factors.
Collections
Details
- License:
- Artistic-2.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Mac, Windows
- Programming Languages:
- R
- Added:
- 8/30/2026
- Last Updated:
- 8/30/2026
Operations
Publications
Documentation
User manual
https://bioconductor.org/packages/compSPOTDownloads
- Source codehttps://github.com/sydney-grant/compSPOT